Choroidoretinal Dystrophy &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; &nbs 858h71i p; 243
General: Sex-linked; similar to retinitis pigmentosa with absence of annular scotoma and little vascular change.
Ocular: Early poor central vision; retinitis pigmentosa; night blindness.
Clinical: None.
Hoare GW. Choroidoretinal dystrophy. Br J Ophthalmol 1965; 49:449-451.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press. 1998.
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