J Korean Ophthalmol Soc.
1989 Oct;30(5):847-853.
The Laurence-Moon-Biedl Syndrome in a Family
- Affiliations
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- 1Department of Ophthalmology, School of Medicine, Inje University, Seoul, Korea.
Abstract
- Laurence-Moon-Biedl syndrome is a rare inherited disorder and its common findings include pigmentary retinal degeneration, obesity, hypogonadism, mental retardation and digital anomaly. Recently, the authors experienced two cases of Laurence-Moon-Biedl syndrome in a family of 15 year-old male and 17 year-old female. In our cases, the male patient showed syndactyly and polydactyly, chorioretinal degeneration, hypogonadism and female patient showed polydactyly, chorioretinal degeneration, hypogonadism, obesity and mental retardation.
