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Case Reports
. 1991 Mar;198(3):207-14.
doi: 10.1055/s-2008-1045954.

[Autosome dominant vitreoretinal dystrophy with skeletal dysplasia in one generation]

[Article in German]
G E Lang  1 , B Laudi, R A Pfeiffer
Affiliations
Case Reports

[Autosome dominant vitreoretinal dystrophy with skeletal dysplasia in one generation]

[Article in German]
G E Lang et al. Klin Monbl Augenheilkd. 1991 Mar.

Abstract

We report on ten patients of four generations with autosomal dominant vitreoretinal dystrophy with different manifestation. The ophthalmological findings are retinal detachment, retinal holes, retinoschisis, lattice and snowflake degeneration, vitreoretinal adhesions, chorioretinal atrophy and peripheral pigment epithelial changes. Two sisters show growth retardation with skeletal anomalies most likely brachyolmia.

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