Article
[Weill Marchesani syndrome. Report of a case].
Journal francais d'ophtalmologie - 1 Nov 2001
el Kettani A, Hamdani M, Rais L, el Belhadji M, Rachid R, Laouissi N, Zaghloul K, Amraoui A
Abstract excerpt
Weill Marchesani syndrome is a congenital disease that combines microspherophakia and skeletal abnormalities. The authors report a 19-year-old male, born of a consanguineous marriage, with a progressive decrease in visual acuity. The general examination showed a squat look, dwarfism, muscle hypertrophy, short hands and feet, and joint stiffness. The ophthalmological examination showed that visual acuity was...
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