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Br J Ophthalmol 81:373-377 doi:10.1136/bjo.81.5.373
  • Original Article
    • Clinical science

Ocular abnormalities in thin basement membrane disease

Table 2

Renal and ocular features of patients with IgA glomerulonephritis or Alport syndrome

(A) IgA glomerulonephritis
Patient Sex Age Haem Pro BP Renal function Cornea Lens Retina
JJ F 37 + + ABN N N N 0 dots
LJ F 64 + + N N dots N 0 dots
JB M 58 + + N ABN N N 100 dots
JM M 39 + + N N N N 0 dots
FE F 46 + + N ABN N N 0 dots
FD F 38 N N N N 0 dots
CL M 23 + N N N N 0 dots
HP M 51 + N N N N 0 dots
TW M 51 + + N ABN N N 0 dots
GJ M 44 + + ABN ABN N N 1 dot
FR F No further details N N 0.5 dots
(B) X linked Alport syndrome
Patient Sex Age (years) FH Hearing Renal function Age at renal failure Cornea Lens Retina
DH M 17 + Abn N, haem NA Corneal dystrophy Dots 1 dot
PH F 45 + N N, haem NA Corneal dystrophy N 0.5 dot
JT F 46 + N N, haem NA N Opacity 6 dots
NH M 30 Abn Transplant 15 Dots Scissor’s reflex Dots and flecks
AC M 34 Abn Transplant 17 N N Dots and flecks
CH F 37 + N N, haem NA N N 1 dot
  • Haem = + RBC greater than × 106/l; Pro = proteinuria + more than 0.3 g/day; BP + = blood pressure more than 140/90 mm Hg; FH = family history; N = normal; Abn = abnormal; NA = not applicable.

  • PH and DH are mother and son; electron microscopy of PH’s renal biopsy was typical of Alport syndrome, but DH has not had a biopsy.

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