Choroideremia.
- Author:
Chul Yong LEE
1
;
Tong Yoll SHIN
Author Information
- Publication Type:Case Report
- MeSH: Atrophy; Choroid; Choroideremia*; Epithelium; Humans; Night Blindness; Retina; X Chromosome
- From:Journal of the Korean Ophthalmological Society 1981;22(2):433-438
- CountryRepublic of Korea
- Language:Korean
- Abstract: Choroideremia is characterized by progressive atrophy of choroid and pigment epithelium of retina leading to night blindness and gross loss of field. and is inherited as X chromosome linked intermediate. Authors experienced 2 cases among a family of choroideremia. The clinical finding and brief reviews of literatures are reported as followings.
