Skip to main content
Log in

Genetics of microphthalmos

  • Published:
International Ophthalmology Aims and scope Submit manuscript

Abstract

This is a survey of the genetics of microphthalmos and the heritable syndromes in which microphthalmos occurs. New syndromes are delineated such as the autosomal dominant anophthalmos-microphthalmos-coloboma syndrome, the autosomal dominant microphthalmos, microcephaly, lacunar retinal atrophy syndrome, the autosomal recessive anophthalmos-microphthalmos-coloboma syndrome, the autosomal recessive syndrome with anophthalmos or microphthalmos and genital malformations, and the autosomal recessive syndrome with microphthalmos, microcephaly and retinal falciform folds. Nanophthalmos is described as a poorly defined phenotype and rejected as a genotype. Several other genetic entities with microphthalmos are reviewed and recent descriptions are surveyed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Adams, C.W. & W.E. Nance. Persistent tachycardia, paroxysmal hypertension, and seizures: Association with hyperglycinuria, dominantly inherited microphthalmia, and cataracts. J.A.M.A. 202: 525–530 (1967).

    Google Scholar 

  2. Aicardi, J., J. Lefebre & A. Lerique-Koechlin. A new syndrome: Spasm in flexion, callosal agenesis, ocular abnormalities. Electroencephalogr. Clin. Neurophysiol. 19: 609–610 (1965).

    Google Scholar 

  3. Aicardi, J. & J.J. Chevrie. Le syndrome agénésie calleuse, spasmes en flexion, lacunes chorio-rétiniennes. Arch. Franc. Ped. 26: 809–810 (1969).

    Google Scholar 

  4. Aicardi, J., J.J. Chevrie & F. Rousselie. Le syndrome spasmes en flexion, agénésie calleuse, anomalies choriorétiniennes. Arch. Franc. Ped. 26: 1103–1120 (1969).

    Google Scholar 

  5. Alkemade, P.P.H. Dysgenesis mesodermalis of the iris and the cornea. Thesis. Van Gorcum & Co. 1969.

  6. Altmann, P., P. Wagenbichler & A. Schaller A casuistic report on the Gruber or Meckel syndrome. Hum. Genet. 38: 357–362 (1977).

    Google Scholar 

  7. Aracena, T. & P. Sangueza. Hallermann-Streiff-Francois syndrome. J. Pediatr. Ophthal. and Strab. 14: 373–378 (1977).

    Google Scholar 

  8. Aula, P., O. Karjalainen, J. Rapola, J. Lindgren & M. Seppälä. Prenatal diagnosis of the Meckel syndrome. Am. J. Obstet. Gynecol. 129: 700–702 (1977).

    Google Scholar 

  9. Azevedo, E.S., J. Biondi & L.M. Ramalho. Cryptophthalmos in two families from Bahia, Brazil. J. Med. Genet. 10: 389–392 (1973).

    Google Scholar 

  10. Bennett, M.E. A study in a case of congenital anophthalmia. Amer. J. Psychother. 27: 529–538 (1973).

    Google Scholar 

  11. Bernard, R., G. Farnarier, F. Giraud, N. Pinsard & Y. Brusquet. A propos de quatre cas d'anopthalmie congénitale. Pediatrie 22: 249–350 (1967).

    Google Scholar 

  12. Bertoni, J.M., S. von Loh & R.J. Allen. The Aicardi syndrome: Report of 4 cases and review of the literature. Ann. Neurol. 5: 475–482 (1979).

    Google Scholar 

  13. Bethge, R., & L.-V. Hörenz. Neue Bobachtung beim oculo-dento-digitalen Syndrom. Beitr. Orthop. Traumatol. 24: 424–431 (1971).

    Google Scholar 

  14. Bianchine, J.W. A family with microphthalmia, anophthalmia and concomitant oligophrenia. Birth Def. Orig. Art. Ser. VII/3: 205–206 (1971).

    Google Scholar 

  15. Bianchine, J.W., M.L. Briard-Guillemot, P. Maroteaux, J. Frézal & H.E. Harrison. Generalized osteoporosis with bilateral pseudoglioma -An autosomal recessive disorder of connective tissue: Report of three families - Review of the literature. Am. J. Hum. Genet. 24: 34a (1972).

  16. Biermann, B. & W.G. Momma. Kryptophthalmie. Fortschr. Kiefer Gesichts chir. 22: 140–141 (1977).

    Google Scholar 

  17. Brandt-Hansen, P.M. Anoftalmus. T. norske Lægeforen. 93: 1780–1781 (1975).

    Google Scholar 

  18. Braun-Falco, O. & C. Hofmann. Das Goltz-Gorlin-Syndrom. Übersicht und Kasuistik. Der Hautartz. 26: 393–400 (1975).

    Google Scholar 

  19. Briard-Guillemot, M.L., H. Saraux, M.F. Blanck & J. Frézal. Dysplasie hyaloïde-rétinienne avec ostéoporose. Etude de deux familles. 4th. Congr. Int. Génét. Hum., Paris 1971. Excerpta med. Int. Congr. Ser., No. 233: 34, 1971, Amsterdam.

  20. Brini, A., A. Pennerath & C. Lausecker. Dysplasie rétinienne bilatérale avec ostéoporose. Bull. Soc. Ophthalm. Fr. 78: 789–793 (1978).

    Google Scholar 

  21. Brockhurst, R.J. Nanophthalmos with uveal effusion. Tr. Am. Ophthal. Soc. 72: 372–403 (1974).

    Google Scholar 

  22. Brownstein, S., T.H. Kirkham & D.K. Kalousek. Bilateral renal agenesis with multiple congenital ocular anomalies. Am. J. Ophthalmol. 82: 770–774 (1976).

    Google Scholar 

  23. Butler, M.G., J.D. Eisen & J. Henry. Cryptophthalmos with an orbital cyst and profound mental and motor retardation. J. Ped. Ophthal. Strab. 15: 233–235 (1978).

    Google Scholar 

  24. Calhoun, F.P. Jr. The management of glaucoma in nanophthalmos. Tr. Am. Ophth. Soc. 73: 97–122 (1975).

    Google Scholar 

  25. Cantú, J.M., J.A. Rojas, D. Garcia-Cruz, A. Hernández, P. Pagán, R. Fragoso & C. Manzano. Autosomal recessive microcephaly associated with chorioretinopathy. Hum. Genet. 36: 243–247 (1977).

    Google Scholar 

  26. Capella, J.A., H.E. Kaufmann, F.J. Lill & G. Cooper. Hereditary cataracts and microphthalmia. Am. J. Ophthalmol. 56: 454–458 (1963).

    Google Scholar 

  27. Carones, A.V. Syndrome dyscéphalique de Francois. Ophthalmologica 142: 510 (1961).

    Google Scholar 

  28. Caronni, E. Un caso di anoftalmo bilaterale cosidetto ‘clinico primario’ con microblefaro. Minerva Chir. 22: 251–254 (1967).

    Google Scholar 

  29. Caspersen, I.& M. Warburg. Hallermann-Streiff syndrome. Acta Ophthalm. (Kbh.) 46: 385–389 (1968).

    Google Scholar 

  30. Cennamo, G., M. Gangemi & A. Magli. Hydrocephalus combined with congenital cataract and microphthalmia. J. Pediatr. Ophthalm. 16: 382–385 (1979).

    Google Scholar 

  31. Chemke, J., B. Czernobilsky, G. Mundel & Y.R. Barishak. A familial syndrome of central nervous system and ocular malformations. Clin. Genet. 7: 1–7 (1975).

    Google Scholar 

  32. Chemke, J., A. Miskin, Z. Rav-Acha, A. Porath, M. Sagiv & Z. Katz. Prenatal diagnosis of Meckel syndrome: alphafeto protein and beta-trace protein in amniotic fluid. Clin. Genet. 11: 285–289 (1977).

    Google Scholar 

  33. Chovet, M., J. Dufour & J. Degabriel. Cryptophtalmies et malformations associées en milieu africain consanguin (Mauritanie du Sud). Médécine Tropicale 32/suppl.: 419–426 (1972).

    Google Scholar 

  34. Chrysostomidou, O.M. et al. Rétino-hyaloid dysplasia with osteoporosis and hypotonia: A syndrome with autosomal recessive transmission in a Greek family. (Abstract) 4th Int. Conf. Birth Def. Vienna 1973. Excerpta Medica interntl. Congr. Ser. 297: 69, 1973 Amsterdam.

  35. Coover, D.H. Two cases of cryptophthalmia. Ophthalmoscope 8: 259 (1910).

    Google Scholar 

  36. Cross, H.E., V.A. McKusick & W. Breen. A new oculocerebral syndrome with hypopigmentation. J. Pediatr. 70: 398 (1967).

    Google Scholar 

  37. Cross, H.E. & F. Yoder. Familial nanophthalmos. Am. J. Ophthalmol. 81: 300–306 (1976).

    Google Scholar 

  38. Cross, H.E. Penetfance and variability in anterior chamber malformations. Birth Def.: Orig. Art. Ser. 15/5B: 131–144 (1979).

    Google Scholar 

  39. Cuendet, J.F. La microphthalmie compliquée. Ophthalmologica 141: 380–385 (1961).

    Google Scholar 

  40. Cummings, C., R.C. Polomeno & P.J. McAlpine. Autosomal dominant cataract, coloboma and microphthalmia. Vth. Intern. Conf. on Birth Def. Montreal 1977.

  41. De Corte, M.T., C. Lambotte & P. Beauduin. Le syndrome de Hallermann - Streiff - Francois ou la dyscéphalie ‘Tête d'oiseau’. Revue Médicale de Liège 27: suppl. 1: 111–116 (1972).

    Google Scholar 

  42. Denden, A. & K. Ahrens. Dysplastische Entwicklungsstörungen im Schädel-Gesichts-Bereich mit Extremitäten-missbildungen. Klin. Monatsbl. Augenheilk. 151: 230–239 (1967).

    Google Scholar 

  43. Dennis, J. & B.D. Bower. The Aicardi syndrome. Developm. Med. and Child Neurol. 14: 382–390 (1972).

    Google Scholar 

  44. Dinno, N.D., W.C. Edwards & B. Weiskopf. The Cryptophthalmos-syndactyly syndrome. Clin. Pediatr. 13: 219–224 (1974).

    Google Scholar 

  45. Dolman, C.L. & V.J. Wright. Necropsy of original case of Lowry's syndrome. J. Med. Genet. 15: 227–229 (1978).

    Google Scholar 

  46. Donders, P.C. Hallermann-Streiff syndrome. Doc. Ophthal. 44, 1: 161–166 (1977).

    Google Scholar 

  47. Dorp, D.B. van & J.W. van Dellemann. A family with X-chromosomal recessive congenital cataract, microphthalmia, a peculiar form of the ear and dental anomalies. J. Pediatr. Ophthal. and Strab. 16: 166–171 (1979).

    Google Scholar 

  48. Dudgeon, J. & I.A. Chisholm. Oculo-dento-digital dysplasia. Trans. Ophthalm. Soc. U.K. 94:/1: 203–210 (1974).

    Google Scholar 

  49. Duke-Elder, S. System of Ophthalmology vol III Henry Kimpton, London 1964, pp. 488–489.

    Google Scholar 

  50. Emberger, J.-M., D. Pincemin, M. Mohieddine & C. Boudet. Cryptophthalmie aspect anantomo-pathologique et génétique. Bull. Soc. Ophtalm. Fr. 76: 545–548 (1976).

    Google Scholar 

  51. Fan, H.-C. Cryptophthalmos. A case report. Chinese Med. J. 79: 172–174 (1959).

    Google Scholar 

  52. Fára, M., I. Horák, J. Hrivnàková, J. Kapras, M. Nová, M. Stloukalova. Oculodentodigital dysplasia. Acta Chir. Plast. (Praha) 19: 110–122 (1977).

    Google Scholar 

  53. Fariello, R.G., R.W.M. Chun, J.M. Doro, R. Buncic & J.S. Prichard. EEG recognition of Aicardi's syndrome. Arch. Neurol. 34: 563–566 (1977).

    Google Scholar 

  54. Farman, A.G., S.N. Smith & C.J. Nortjé. Oculodento-digital dysplasia. Brit. Dent. J. 142: 405–408 (1977).

    Google Scholar 

  55. Fitch, N. & L. Pinsky. The Meckel syndrome with limited expression in relatives. Clin. Genet. 4: 33–37 (1973).

    Google Scholar 

  56. Fitch, N. & M. Kaback. The Axenfeld syndrome and the Rieger syndrome. J. Med. Genet. 15: 30–34 (1978).

    Google Scholar 

  57. Fraccaro, M., G. Morone, U. Manfredini & R. Sanger. X-linked cataract. Ann. Hum. Genet. 31: 45–50 (1967).

    Google Scholar 

  58. Francheschetti, A. & H. Gernet. Diagnostique ultrasonique d'une microphthalmie sans microcornée, avec macrophakie, haute hypermétropie associée a une dégénérescence tapéto-rétinienne, une disposition glaucomateuse et des anomalies dentaires. Arch. Ophtal. (Paris) 25: 105–116 (1965).

    Google Scholar 

  59. François, J. A'propos d'une famille présentant des anomalies oculaires du type colobomateux depuis le colobome unilatéral de l'iris jusqu'a l'anophthalmie bilatérale, associée au syndrome de Bardet-Biedl. J. Génétique hum. 2: 203–218 (1953).

    Google Scholar 

  60. François, J. A new syndrome. Dyscephalia with bird face and dental anomalies, nanism, hypotrichosis, cutaneous atrophy, microphthalmia and congenital cataract. Arch. Ophthal. 60: 842–862 (1958).

    Google Scholar 

  61. François, J. L'Hérédité en Ophtalmologie. Masson et Cie, Paris 1958, pp. 190–191.

    Google Scholar 

  62. François, J. Syndrome malformatif avec cryptophthalmie. Note préliminaire. Ophthalmologica 150: 215–218 (1965).

    Google Scholar 

  63. François, J. Malformative syndrome with cryptophthalmia. In Francois, J. and Gordon, D.M. (Eds.) Genetic Aspects of Ophthalmology Internat. Ophthalmology Clinics vol. 8, no. 4, 817–837, Little Brown and Co. Boston 1968.

    Google Scholar 

  64. François, J. Syndrome malformatif avec cryptophthalmie. Acta Genet. Med. Gemellol. 18: 18–50 (1969).

    Google Scholar 

  65. Fraser, G.R. & A. Friedmann. The Causes of Blindness in Childhood. Johns Hopkins Hosp. Press, Baltimore, 1967.

    Google Scholar 

  66. Fraser, G.R. & A.I. Friedmann. The causes of Blindness in Childhood. The Johns Hopkins Press, Baltimore 1967 (p. 59–60).

    Google Scholar 

  67. Freedom, R.M. The asplenia syndrome: A review of significant extracardiac structural abnormalities in 29 necropsied patients. J. Pediat. 81: 1130–1133 (1972).

    Google Scholar 

  68. Friedman, M.W. & E.S. Wright. Hereditary microcornea and cataract in five generations. Am. J. Ophthalmol. 35: 1017–1021 (1952).

    Google Scholar 

  69. Friedrich, U., K.B. Hansen, M. Hauge, I. Hägerstrand, K. Kristoffersen, E. Ludvigsen, U. Merrild, B. Nørgård-Pedersen, G.B. Petersen & A.J. Therkelsen. Prenatal diagnosis of polycystic kidneys and encephalocele (Meckel syndrome) Clin. Genet. 15: 278–286 (1979).

    Google Scholar 

  70. Gartner, S. Congenital retinal folds and microcephaly. Arch. Ophth. 25: 93–100 (1941).

    Google Scholar 

  71. Gerhard, J.-P., J.-G. Juif, J.-Cl. Luckel & Mack. A propos dúne nouvelle observation de syndrome de spasme en flexion, agénésie calleuse et anomalies chorio-rétiniennnes (syndrome Aicardi). Bull. Soc. Ophtal. Fr. 73: 363–366 (1973).

    Google Scholar 

  72. Gerhard, J.-P., A. Brini, D. Willard & S. Guez. Décollement rétinien total bilatéral avec microphthalmie. Discussion de la valeur clinique d'une hydrocephalie associée. Bull. Soc. Ophtalm. Fr. 76: 645–647 (1976).

    Google Scholar 

  73. Ginsburg, L.D., H.O. Sedano & R.J. Gorlin. Focal dermal hypoplasia syndrome. Am. J. Roentgenology, Radium Ther. and Nuclear Med. 110: 561–571, 1970.

    Google Scholar 

  74. Goldberg, H.G. Cryptophthalmus: Congenital ankyloblepharon. Ophthalmol. Rec. 21: 200 (1912).

    Google Scholar 

  75. Goldberg, M. & V.A. McKusick. X-linked colobomatous microphthalmos and other congenital anomalies. Am. J. Ophthalmol. 71: 1128–1133 (1971).

    Google Scholar 

  76. Goldberg, M.F. & J. Hardy. X-linked cataract. Birth Def. Orig. Art. Ser. 7/3: 164–165 (1971).

    Google Scholar 

  77. Goldhammer, Y. & J.L. Smith. Cryptophthalmos syndrome with basal encephaloceles. Am. J. Ophthalmol. 80: 146–149 (1975).

    Google Scholar 

  78. Goltz, R.W., W.C. Peterson, R.J. Gorlin & H.G. Ravits. Focal dermal hypoplasia. Arch. Dermat. 86: 708–717 (1962).

    Google Scholar 

  79. Goltz, R.W., R.R. Henderson, J.H. Hitch & J.E. Ott. Focal dermal hypoplasia syndrome. A review of the literature and report of two cases. Arch. Derm. 101: 1–11 (1970).

    Google Scholar 

  80. Goravalingappa, J.P. & H.K. Nashi. Congenital malformations in a study of 2398 consecutive births. Indian J. Med. Res. 69: 140–146 (1979).

    Google Scholar 

  81. Gorlin, R.J., A.P. Chaudhry & M.L. Moss. Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies - a new syndrome? J. Pediat. 56: 778–785 (1960).

    Google Scholar 

  82. Gorlin, R.J., L.H. Meskin, W.C. Peterson Jr. & R.W. Goltz. Focal dermal hypoplasia syndrome. Acta DermVenerol. (Stockh.) 43: 421–440 (1963).

    Google Scholar 

  83. Gorlin, R.J. & H. Sedano. Cryptophthalmia syndrome. Modern Medicine November 3: 156–157 (1969).

    Google Scholar 

  84. Gorlin, R.J., J.J. Pindborg & M.M. Cohen. Syndromes of the Head and Neck. McGraw-Hill. New York etc. 1976 (2nd edition).

    Google Scholar 

  85. Gottlieb, S.K., B.K. Fisher & G.A. Violin. Focal dermal hypoplasia. Arch. Dermat. 108: 551–553 (1973).

    Google Scholar 

  86. Gragg, G.W. X-linked cataract. Birth Def. Orig. Art. Ser. 7/3: 164–165 (1971).

    Google Scholar 

  87. Grizzard, W.S., J.J. O'Donnell & J.C. Carey. The cerebrooculo-facio-skeletal syndrome. Am. J. Ophthalmol. 89: 293–298 (1980).

    Google Scholar 

  88. Gruber, G.B. Beiträge zur Frage ‘gekoppelter’ Missbildungen. Beitr. path. Anat. 93: 459 (1934).

    Google Scholar 

  89. Haines, J.O. & S.C. Rogers. Oculodento-digital dysplasia: a rare syndrome. Brit. J. Radiology 48: 932–936 (1975).

    Google Scholar 

  90. Halbertsma, K.T.A. Familiaire aangeboren cataract. Ned. Tijds. Geneesk. 1705 (1934).

  91. Hallermann, W. Vogelgesicht und cataracta congenita. Klin. Monatsbl. Augenheilk. 113: 315–318 (1948).

    Google Scholar 

  92. Hammami, H., E.B. Streiff & E. de Wolff. Contribution á la connaissance du syndrome d'Aicardi et coll. Bull. Mém. Soc. Fr. Ophtal. 85: 598–614 (1972).

    Google Scholar 

  93. Harman, N.B. Congenital cataract, a pedigree of five generations. Trans. Ophthalm. Soc. U.K. 29: 101–108 (1909).

    Google Scholar 

  94. Harms, W.A. Congenital miosis associated with sex-linked congenital cataracts. J. Kansas Med. Soc. 78: 497–502 (1977).

    Google Scholar 

  95. Hauschild, E. Beitrag zur Haufigheit, Erscheinungsform und Aetiologie des Mikrophthalmus (M.) Acta Ophthal. (Kbh.), 47: 926–936 (1969).

    Google Scholar 

  96. Heinemann, M.-H., R. Breg & E. Cotlier. Rieger's syndrome with pericentric inversion of chromosome 6. Brit. J. Ophthalm. 63: 40–44 (1979).

    Google Scholar 

  97. Henkind, P., I.M. Siegel & R.E. Carr. Mesodermal dysgenesis of the anterior segment: Rieger's anomaly. Arch. Ophthalm. 73: 810–817 (1965).

    Google Scholar 

  98. Hermann, P. Le syndrome microphtalmie-rétinite pigmentaire-glaucome. Arch. Ophtal. (Paris) 18: 17–24 (1958).

    Google Scholar 

  99. Hoefnagel, D., M.E. Keenan & F.H. Allen. Heredofamilial bilateral anophthalmia. Arch. Ophthal. 69: 760–764 (1963).

    Google Scholar 

  100. Holmes, L.B. & D.S. Walton. Hereditary microcornea, glaucoma, and absent frontal sinuses: A family study. J. Pediatr. 74: 968–972 (1969).

    Google Scholar 

  101. Hopkins, D.J. The association of bilateral clinical anophthalmos with familial and multiple ocular defects. J. Pediatr. Ophthal. 7: 92–94 (1970).

    Google Scholar 

  102. Hopkins, D.J. & E.C. Horan. Glaucoma in the Hallermann-Streiff syndrome. Brit. J. Ophthal. 54: 416–422 (1970).

    Google Scholar 

  103. Horan, M.B. & F.A. Billson. X-linked cataract and Hutchinsonian teeth. Aust. Paediat. J. 10: 98–102 (1974).

    Google Scholar 

  104. Howard, R.O., R.M. Fineman, B. Anderson, N. Moseley, M. Gilman & S. Rothman. Unilateral cryptophthalmia. Am. J. Ophthalmol. 87: 556–560 (1979).

    Google Scholar 

  105. Hoyt, C.S., F. Billson R. Ouvrier & G. Wise. Ocular features of Aicardi's syndrome. Arch. Ophthal. 96: 291–295 (1978).

    Google Scholar 

  106. Hsia, Y.E., M. Bratu & A. Herbordt. Genetics of the Meckel syndrome (Dysencephalia splanchnocystica) Pediatr. 48: 237–247 (1971).

    Google Scholar 

  107. Hussels, I.E. Midface syndrome with iridochoroidal coloboma and deafness in a mother: microphthalmia in her son. Birth Def. Orig. Art. Ser. 7/7: 269 (1971).

    Google Scholar 

  108. Ide, C.H. & P.B. Wollschlaeger. Multiple congenital abnormalities associated with cryptophthalmia. Arch. Ophthalm. 81: 638–644 (1969).

    Google Scholar 

  109. Ishak, M. Consecutive anophthalmos and cryptophthalmos. Bull. Ophthal. Soc. Egypt. 68: 489–491 (1975).

    Google Scholar 

  110. Ishwarchandra & J.S. Mulak. Bilateral cryptophthalmos (Ablepharon). J. All-India Ophthal. Soc. 14: 225–226 (1966).

    Google Scholar 

  111. Jalbert, P., Y. Gilbert, P. Leopold, C. Mouriqand & A. Beaudoing. Syndrome d'Hallermann-Streiff-Francois. A propos d'une nouvelle observation associé a une anomalie caryotypique 4p-. Pédiatrie 23: 703–705 (1968).

    Google Scholar 

  112. Jessner, M. Naeviforme, poikilodermie-artige Hautveränderungen mit Missbildungen (Schwimmhautbildung an den Fingern. Papillome am Anus). Zbl. Hautu. Geschl.- Kr 27: 468 (1927).

    Google Scholar 

  113. Jong, J.G.Y. de, J.W. Delleman, M. Houben, W.A. Manchot, A. de Minjer, J. Mol & J.L. Sloof. Agenesis of the corpus callosum, infantile spasms, ocular anomalies (Aicardi's syndrome). Neurology 26: 1152–1158 (1976).

    Google Scholar 

  114. Jorgenson, R.J., L.S. Levin, H.E. Cross, F. Yoder & T.E. Kelly. The Rieger syndrome. Am. J. Med. Genet. 2: 307–318 (1978).

    Google Scholar 

  115. Jorgenson, R.J., F.E. Yoder & L.S. Levin. The Rieger syndrome. J. Med. Genet. 16: 236–237 (1979).

    Google Scholar 

  116. Joshi, N.D. Two cases of cryptophthalmus. Acta Soc. Ophthal. Japon. 72: 179–181 (1968).

    Google Scholar 

  117. Judge, C. & J.E. Chakanovskis. The Hallermann-Streiff syndrome. J. ment. Def. Res. 15: 115–120 (1971).

    Google Scholar 

  118. Judge, C. A sibship with the pseudothalidomide syndrome and an association with Rh incompatibility. Med. J. Austr. 2: 280–281 (1973).

    Google Scholar 

  119. Judisch, G.F., A. Martin-Casals, J.W. Hanson & W.H. Olin. Oculodentodigital dysplasia. Four new reports and a literature review. Arch. Ophthal. 97: 878–884 (1979).

    Google Scholar 

  120. Kadrnka-Lovrenčič, M., S. Jurkovič, ZŬ Reiner-Banovac, E. Najman & M. Lovrenčič. Die oculo-dento-digitale Dysplasie (Das Meyer-Schwiekerath-Syndrom). Mschr. Kinderheilk. 121: 595–599 (1973).

    Google Scholar 

  121. Kaffe, S., J.S. Rose, L. Godmilow, B.A. Walker, T. Kerenyi, N. Beratis, P. Reyes & K. Hirschhorn. Prenatal diagnosis of renal anomalies. Am. J. Med. Genet. 1: 241–251 (1977).

    Google Scholar 

  122. Kapoor, S. & M. Kapoor. Congenital ocular anomalies in Pondicherry. J. Pediatr. Ophthal. 14: 382–389 (1977).

    Google Scholar 

  123. Kapoor, S. Otolaryngological features of Malformation syndrome with cryptophthalmos. J. Laryng. Otol. 93: 519–525 (1979).

    Google Scholar 

  124. Karel, I., E. Sedláčková, J. Komínek & Kolář. Dysplasia oculodentodigitalis. Cs. Oftalmologie 25: 88–97 (1969).

    Google Scholar 

  125. Kimball, M.E., A. Milunski & E. Alpert. Prenatal diagnosis of neural tube defects III. A re-evaluation of the alphafetoprotein assay. Obstetrics and Gynecology. 49: 532–536 (1977).

    Google Scholar 

  126. Kimbrough, R.L., C.S. Trempe, R.J. Brockhurst & R.J. Simmons. Angle-closure glaucoma in nanopthalmos. Am. J. Ophthdmol. 88: 572–579 (1979).

    Google Scholar 

  127. Koch, G. Genealogisch-demographische Untersuchungen über Mikrocephalie in Westphalen. Forschungsberichte des Landes Nord Rhein-Westphalen. 1963: 99–100 (1968).

    Google Scholar 

  128. Krill, A.E., G. Woodbury & J.E. Bowman. X-chromosomal linked sutural cataracts. Am. J. Ophthalmol. 68: 867–872 (1969).

    Google Scholar 

  129. Kupfer, C. & M.I. Kaiser-Kupfer. New hypothesis of developmental anomalies of the anterior chamber associated with glaucoma. Trans. ophthal. Soc. 98: 213–215 (1978).

    Google Scholar 

  130. Lechot, N.J., J.J. Nef, M.J. Becker-Bloemkolk, M. Verjaal & P.F. Wiesenhaan. Prenatal diagnosis of Meckel syndrome. Hum. Genet. 43: 333–336 (1978).

    Google Scholar 

  131. Lenz, W. Recessiv-geschlechtsgebundene Mikrophthalmie mit multiplen Missbildungen. Zeitschr. f. Kinderheilk., 77: 384–390 (1955).

    Google Scholar 

  132. Lindstedt, E. Congenital malformations of the eye. Acta Ophthal. (Kbh.) 46: 355–359 (1968).

    Google Scholar 

  133. Loewer-Sieger, D.H., J.W. Delleman, A.W.C. van Veelen, P. Fleury & J.B. Bijlsma. Microcephaly, mental retardation and chorioretinopathy. Ophthalmologica 176: 279–280 (1978).

    Google Scholar 

  134. Lohmann, W. eitrag zur Kenntnis des reinen Mikrophthalmus. Arch. Augenheilk. 36: 136–141 (1920).

    Google Scholar 

  135. Lurie, I.W., E.D. Cherstvoy, G.I. Lazjuk, M.K. Nedzved & S.S. Usoev. Further evidence for the autosomal-recessive inheritance of the COFS syndrome. Clin. Genet. 10: 343–346 (1976).

    Google Scholar 

  136. Mabrouck, R., A. Chadli, H. Djedidi & T.B. Cheikh. A propos de 4 cas de kyste orbito-papébral colobomateaux. Bull. Soc. Fr. d'Optalm. 81: 173–191 (1968/1969).

    Google Scholar 

  137. MacRae, D.W., R.O. Howard, D.M. Albert & Y.E. Hsia. Ocular manifestations of the Meckel syndrome. Arch. Ophth. 88: 106–113 (1972).

    Google Scholar 

  138. Magruder, A.C. Cryptophthalmus. Am. J. Ophthalm. 4: 48 (1921).

    Google Scholar 

  139. Majeski, J.A. Asplenia associated with a congenital diaphragmatic defect and neurologic anomalies. South. Med. J. 71: 1447–1448 (1978).

    Google Scholar 

  140. Masuda, Y. Two cases of albatio falciformis congenita and two other cases of ocular congenital anomalies, which appeared in a pedigree with consanguineous marriages. J. Clin. Ophthal., Tokyo 16: 325 (1962); cited by Ricci (1969).

    Google Scholar 

  141. Matsoukas, J., S. Liarikos, A. Giannikas, Z. Agoropoulos, G. Papachristou & P. Soukakos. A newly recognized dominantly inherited syndrome: short stature, ocular and articular anomalies, mental retardation. Helv. Paediatr. Acta 28: 383–386 (1973).

    Google Scholar 

  142. McKusick, V.A., M. Stauffer, D.L. Knox & D.B. Clark. Chorioretinopathy with hereditary microcephaly. Arch. Ophthal. 75: 597–600 (1966).

    Google Scholar 

  143. McKusick, V.A. Heritable Disorders of Connective Tissue. 4th. ed. Mosby, St. Louis 1972.

    Google Scholar 

  144. McKusick, V.A. Mendelian Inheritance in Man. Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes; 5th. ed Hopkins University Press, Baltimore. 1978.

    Google Scholar 

  145. Mecke, S. & E. Passarge. Encephalocele, polycystic kidneys, and polydactyly as an autosomal recessive trait simulating certain other disorders: The Meckel syndrome. Ann. Génét. 14: 97–103 (1971).

    Google Scholar 

  146. Meckel, J.F. Beschreibung tweier durch sehr ähnliche Bildungsabweichungen entstellter Geschwister. Dtsch. Arch. f.d. Physiolog. 7: 99 (1822).

    Google Scholar 

  147. Melchionda, C. Anoftalmia clinica bilaterale familiare. Ann. di Ottalmol. e Clin. Oculist. 93: 309–316 (1967).

    Google Scholar 

  148. Meyer-Schwickerath, G., E. Grüterich & H. Weyers. Mikrophthalmussyndrome. Kl. M.bl. Augenheilk. 131: 18–30 (1957).

    Google Scholar 

  149. Michaels, D.D. & G.S. Zugsmith. Bilateral anophthalmos. Am. J. Ophthalmol. 55: 1256–1259 (1963).

    Google Scholar 

  150. Milunski, A. & E. Alpert. Prenatal diagnosis of neural tube defects. Obstet. Gynecol. 48: 1–5 (1976).

    Google Scholar 

  151. Nance, W.E., M. Warburg, D. Bixler & E.M. Helveston. Congenital sex-linked cataract, dental anomalies and brachymetacarpalia. Birth Def. Orig. Art. Ser. X/4: 285–291 (1974).

    Google Scholar 

  152. Neuhäuser, G., E.G. Kaveggia, & J.M. Opitz. Autosomal recessive syndrome of pseudogliomatous blindness, osteoporosis and mild mental retardation. Clin. Genet. 9: 324–332 (1976).

    Google Scholar 

  153. Nevin, N.C., B.G. Scally, P. Thomas & D.C. Kernohan. The Hallermann-Streiff Syndrome. J. Ment. Defic. Res. 18: 145–151 (1974).

    Google Scholar 

  154. Nevin, N.C., W. Thompson, G. Davison & W.T. Horner. Prenatal diagnosis of the Meckel syndrome. Clin. Genet. 15: 1–4 (1979).

    Google Scholar 

  155. Ogunye, O.O., R.F. Murray & T. Osgood. Linkage studies in Lenz microphthalmia. Hum. Hered. 25: 493–500 (1975).

    Google Scholar 

  156. Opitz, J.M. & J.J. Howe. The Meckel syndrome (Dysencephalia Splanchnocystica, the Gruber syndrome): Birth Def.: Orig. Art. Ser. V/2: 167–169 (1969).

    Google Scholar 

  157. Pagon, R.A., J.W. Chandler, W.R. Collié, S.K. Clarren, J. Moon, S.A. Minkin & J.G. Hall. Hydrocephalus, agyria, retinal dysplasia, encephalocele (HARD ± E) syndrome: An autosomal recessive condition. Birth Def.: Orig. Art. Ser. XIV/6B: 233–241 (1978).

    Google Scholar 

  158. Passarge, E. & S. Fuchs-Mecke. MM-Oculocerebral syndrome with hypopigmentation. Birth Def.: Orig. Art. Ser. XI/2: 466–467 (1975).

    Google Scholar 

  159. Pearce, W.G., S. Nigam & J. Rootman. Primary anophthalmos: Clinical and genetic features. Canad. J. Ophthalm. 9: 141–145 (1974).

    Google Scholar 

  160. Pena, S.D.J. & M.H.K. Shokeir. Autosomal-recessive cerebro-oculo-facio-skeletal (COFS) syndrome. Clin. Genet. 5: 285–293 (1974).

    Google Scholar 

  161. Penner, H. & H.G. Schlack. Anophthalmie und begleitende Fehlbildungen. Klin. Pädiatrie 188: 320–327 (1976).

    Google Scholar 

  162. Pfeiffer, R.A., F. Majewski & H. Mannkopf. Das syndrom von Mohr und Claussen. Klin. Pädiat. 184: 224–229 (1972).

    Google Scholar 

  163. Pierard, J. & J. François. Le syndrome dyscephalique de Francois. Ses rapports avec le tissu élastique. Arch. Belg. Dermat. Syphil. 25: 439–454 (1969).

    Google Scholar 

  164. Pinsky, L., A.M. Di George, R.D. Harley & H.W. Baird. Microphthalmos, corneal opacity, mental retardation and spastic cerebral palsy. An oculo-cerebral syndrome. J. Pediatr. 67: 387–398 (1965).

    Google Scholar 

  165. Piussan, C., B. Cuvelier, C. Lenaerts, B. Ee Mareschal, C. Reguet & B. Risbourg. Ee syndrome cerebro-oculo-facio-squelettique. Arch. Fr. Pédiat. 36: 379–386 (1979).

    Google Scholar 

  166. Poradowska, W. & M. Jaworska. Oral-facial-digital syndrome. Acta Chir. Plast. (Poland) 9: 168–175 (1967).

    Google Scholar 

  167. Preus, M., P. Kaplan & T.H. Kirkham. Renal anomalies and oligohydramnios in the cerebro-oculo-facial-skeletal syndrome. Am. J. Dis. Child. 131: 62–64 (1977).

    Google Scholar 

  168. Priess, G. & M. Teuscher. Klinischer Beitrag zum Hermann-Syndrom. Folia Ophthal. 2: 53–57 (1977).

    Google Scholar 

  169. Rains, D.E., D.A. McCoy & E.J. Nelson. Bilateral microphthalmos in monozygous twins. Ann. Ophthal. 4: 646–652 (1972).

    Google Scholar 

  170. Reinecke, R.D. Cryptophthalmos. Arch. Ophthal. 85: 376–377 (1978).

    Google Scholar 

  171. Reisner, S.H., E. Kott, B. Bornstein et al. Oculodento-digital dysplasia. Am. J. Dis. Child. 118: 600–607 (1969).

    Google Scholar 

  172. Romano, A., R. Tadmor, I. Frank, A. Zaretzky, M. Blumenthal, R. Stein & R.M. Goodman. Clinical and genetic considerations in familial anopthalmia. Metabol. Ophthal. 2: 197–200 (1978).

    Google Scholar 

  173. Ruiz-Maldonado, R., A. Carnevale, L. Tamayo & E.M. Montiel. Focal dermal hypoplasia. Clin. Genet. 6: 36–45 (1974).

    Google Scholar 

  174. Saraux, H., J. Frézal, C. Roy, J.J. Aron, B. Hayat & M. Lamy. Pseudo-gliome et fragilité osseuse héréditaire a transmission autosomale-récessive. Ann. Oculist. (Paris) 200: 1241–1252 (1967).

    Google Scholar 

  175. Saraux, H., H. Miller, J. Mawas, E. Mawas & F. Prépin. La dysplasie hyaloïdo-rétinienne (pseudogliome) a hérédité récessive autosomale. Ann. Oculist. 202: 1131–1137 (1969).

    Google Scholar 

  176. Schanzlin, D.J., D.B. Goldberg & S.E Brown. Hallermann-Streiff syndrome associated with sclerocornea, aniridia and a chromosomal abnormality. Am. J. Ophthalmol. 90: 411–415 (1980).

    Google Scholar 

  177. Schappert-Kimmijser, J. (Chairman) Causes of severe visual impairment in children and their prevention: The Commitee for special study of severe visual impairment in children of the International Association for the Prevention of Blindness. Doc. Ophthal. 39: 213–364 (1975).

    Google Scholar 

  178. Schlieter, F. & U. Schroeder. Über eine Korrelation verschiedener dominant vererbter Augenleiden. Untersuchungen einer Familie mit Mikrocornea, hochgradiger Myopie, Retinitis pigmentosa, Katarakt und Glaucom. Klin. Monatsbl. Attgenheilk. 164: 485–489 (1974).

    Google Scholar 

  179. Schönenberg, H. Kryptophthalmus-Syndrom. Klin. Pädiatr. 185: 165–172 (1973).

    Google Scholar 

  180. Seller, M.J. Case report: Prenatal diagnosis of a neural tube defect: Meckel syndrome. J. Med. Genet. 12: 109–110 (1975).

    Google Scholar 

  181. Seller, M.J. Meckel syndrome and the prenatal diagnosis of neural tube defects. J. Med. Genet. 15: 462–465 (1978).

    Google Scholar 

  182. Shapiro, E.J., M.M. Kaback, K.E. Toomey, D. Sarti, P. Euther & E. Cousins. Prenatal diagnosis of the Meckel syndrome: Use of serial ultrasound and alpha-fetoprotein measurements. Birth. Def. Orig. Art. Ser. XIII/3D: 267–272 (1977).

    Google Scholar 

  183. Silver, H.K., W.C. Blair & C.H. Kempe. Fanconi syndrome. Amer. J. Dis. Child. 83: 14–25 (1952).

    Google Scholar 

  184. Silver, J. & F.W. Hughes. The relationship between morphogenetic cell death and the development of congenital anophthalmia. J. Comp. Neurol. 157: 281–302 (1974).

    Google Scholar 

  185. Sjögren, T. & T. Larsson. Miorophthalmos and anophthalmos with and without coindicent oligophrenia. Munksgaard Cph. 1949.

  186. Steele, R.W. & J.W. Bass. Hallermann-Streiff syndrome. Amer. J. Dis. Child. 120: 462–465 (1970).

    Google Scholar 

  187. Streiff, E.B. Dysmorphie mandibulo-faciale (Tête d'oiseau) et altérations oculaires. Ophthalmologica 120: 79–83 (1950).

    Google Scholar 

  188. Sršeń, S. Congenital anophthalmos in two siblings. Acta Univ. Carol (Med. Monogr.) (Praha) 56: 136–139 (1973).

    Google Scholar 

  189. Sugar, H.S., J.P. Thompson & J.D. Davis. The oculodento-digital syndrome. Am. J. Ophthalmol. 61: 1448–1451 (1966).

    Google Scholar 

  190. Sugar, H.S. Oculodentodigital dysplasia syndrome with angle-closure glaucoma. Am. J. Ophthalmol. 86: 36–38 (1976).

    Google Scholar 

  191. Surana, R.B., J.R. Fraga & S.M. Sinkford. The cerebro-oculo-facio-skeletal syndrome. Clin. Genet. 13: 486–488 (1978).

    Google Scholar 

  192. Temtamy, S.A. & B.A. Shalash. Genetic heterogeneity of the syndrome: microphthalmia with congenital cataract. Birth Def.: Orig. Art. Ser. X/4: 292–293 (1974).

    Google Scholar 

  193. Thodén, C.-J., S. Ryöppy & P. Kuitunen. Oculodentodigital dysplasia syndrome. Acta Paediatr. Scand. 66: 635–638 (1977).

    Google Scholar 

  194. Thomas, J.V., M.O. Yoshizumi, C.K. Beyer, J.L. Craft & D.M. Albert. Ocular manifestations of focal dermal hypoplasia syndrome. Arch. Ophthal. 95: 1997–2001 (1977).

    Google Scholar 

  195. Torczynski, E., F.A. Jacobiec, M.C. Johnston, R.L. Font & J.A. Madewell. Synophthalmia and cyclopia: a histopathologic, radiographic and organogenetic analysis. Doc. Ophthal. 44: 311–378 (1977).

    Google Scholar 

  196. Townes, P.L. B.P. Wood & J.V. McDonald. Further heterogenity of the oral-facila-digital syndrome. Am. J. Dis. Child. 130: 548–554 (1976).

    Google Scholar 

  197. Usher, C.H. A pedigree of microphthalmia with myopia and corectopia. Br. J. Ophthal. 5: 289–299 (1921).

    Google Scholar 

  198. Varnek, L. Cryptophthalmos, dyscephaly, syndactyly and renal aplasia. Acta Ophthalm. (Kbh.) 56: 302–313 (1978).

    Google Scholar 

  199. Waardenburg, P.J. in P.J. Waardenburg, A. Franceschetti & D. Klein. Genetics and Ophthalmology, vol. I., Royal Van Gorcum, Netherlands 1961.

    Google Scholar 

  200. Walsh, F.B. & M.E. Wegman. A pedigree of hereditary cataract, illustrating sex-limiting type. Bull. Johns Hopkins Hosp. 6: 125–135 (1937).

    Google Scholar 

  201. Warburg, M. Focal dermal hypoplasia. Acta Ophthalm. (Kbh.) 48: 525–536 (1970).

    Google Scholar 

  202. Warburg, M. Random inactivation of the X chromosome in intermediate X-linked retinitis pigmentosa. Two hypotheses. Tr. Ophth. Soc. U.K. XCI: 553–560 (1971).

    Google Scholar 

  203. Warburg, M. Hydrocephaly, congenital retinal nonattachment, and congenital falciform fold. Am. J. Ophthalmol. 85: 88–94 (1978).

    Google Scholar 

  204. Waring, G.O. & J.A. Shields. Partial unilateral cryptophthalmos with syndactyly, brachydactyly and renal anomalies. Am. J. Ophthalmol. 97: 437–440 (1975).

    Google Scholar 

  205. Weleber, R.G., E.W. Lovrien & J.B. Isom. Aicardi's syndrome. Case report, clinical features and electrophysiologic studies. Arch. Ophthal. 96: 285–290 (1978).

    Google Scholar 

  206. Wesley, R.K., J.D. Baker & A.L. Golnick. Rieger's syndrome (Oligodontia and primary mesodermal dysgenesis of the iris). Clinical features and report of an isolated case J. Pediat. Ophthal. 15: 67–70 (1978).

    Google Scholar 

  207. Willetts, G.S. Focal dermal hypoplasia. Brit. J. Ophthal. 58: 620–624 (1974).

    Google Scholar 

  208. Wolter, J.R. & D.H. Jones. Spontaneous cataract absorption in Hallermann-Streiff syndrome. Ophthalmologica 150: 401–408 (1965).

    Google Scholar 

  209. Yoshioka, H., T. Sugita & M. Ryu. Nanophthalmos with uveal effusion. The Kurume Med, J. 23: 219–230 (1976).

    Google Scholar 

  210. Zach, G.A. Oculodento-osseous dysplasia syndrome. Oral Surg., 40: 122–125 (1975).

    Google Scholar 

  211. Zehender, W. & Manz. Eine Missgeburt mit hautüberwachsenen Augen oder Kryptophthalmus. Klin. Mbl. Augenheilk. 10: 225–249 (1872).

    Google Scholar 

  212. Zeiter, H.J. Congenital microphthalmos. A pedigree of four affected siblings and an additional report of fortyfour sporadic cases. Am. J. Ophthalmol. 55: 910–922 (1963).

    Google Scholar 

  213. Zingirian, M., A. Liotta & A. Iester. Anoftalmia congenita bilaterale associata a notevole deficit psicomotorio. Ann. Ottal. Clin. Oculist. 93: 291–299 (1967).

    Google Scholar 

  214. Alzial, C., J.L. Dufier, J. Aicardi, J. de Grouchy & H. Saraux. Ocular abnormalities of true microcephaly. Ophthalmologica 180: 333–339 (1980).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Warburg, M. Genetics of microphthalmos. Int Ophthalmol 4, 45–65 (1981). https://doi.org/10.1007/BF00139580

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00139580

Keywords

Navigation