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Norrie disease. Diagnosis of a simplex case by DNA analysis
E W Chynn1, D S Walton, L B Hahn
1Department of Ophthalmology, Massachusetts Eye and Ear Infirmiary, Boston, USA.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|September 1, 1996
Abstract:
Norrie disease is a rare, X-linked recessive disorder characterized by congenital blindness due to malformed retinas. We describe a simplex patient who had leukokoria and whose clinical diagnosis was confirmed only after molecular genetics analysis. DNA analysis was also used to determine the carrier status of relatives of the proband.