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Br J Ophthalmol 83:919-922 doi:10.1136/bjo.83.8.919
  • Original Article
    • Clinical science

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

Table 1

Clinical features of affected members of microphthalmia family

Patient No Age (years) Visual acuity Axial length
(mm, R/L) 		Corneal involvement IOP (R/L)
VI:4 1 PL 14.6/15.4 opaque 41.5/41.5
V:6 28 PL 15.9/20.8 opaque, vascularised, anterior staphyloma 34.5/41.5
V:4 33 no PL 14.7/8.0 opaque, vascularised, left sclerocornea 41.5/41.5
V:3 35 no PL — opaque, vascularised, anterior staphyloma 41.5/41.5
V:1 39 PL 19.2/18.2 opaque, vascularised, anterior staphyloma 12.2/17.3
IV:8 40 PL 10.0/8.5 complete sclerocornea right/left 17.3/17.3
IV:5 41 no PL — opaque, vascularised 41.5/17.3
IV:4 48 PL — opaque, vascularised 17.3/10.2

  • PL = perception of light; IOP = intraocular pressure measured by Schiotz tonometry and converted to mm Hg.

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