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[Vitreoretinochoroidal heredo-dystrophy, microcornea, glaucoma and cataract]
P François1, B Puech, J C Hache
1Clinique Ophtalmologique de Lille, CHRU.
Journal Francais D'Ophtalmologie
|January 1, 1993
Summary
This study identifies a distinct autosomal dominant vitreoretinochoroidopathy, characterized by microcornea and vitreoretinochoroidal dystrophy. Ocular hypertension and cataract are identified as secondary complications of this hereditary condition.
Area of Science:
- Ophthalmology
- Genetics
- Medical Science