The Laurence-Moon-Biedl Syndrome in a Family
Journal of the Korean Ophthalmological Society
;
: 847-853, 1989.
Article
in Korean
| WPRIM
| ID: wpr-93188
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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Retinal Degeneration
/
Polydactyly
/
Syndactyly
/
Hypogonadism
/
Laurence-Moon Syndrome
/
Intellectual Disability
/
Obesity
Limits:
Adolescent
/
Female
/
Humans
/
Male
Language:
Korean
Journal:
Journal of the Korean Ophthalmological Society
Year:
1989
Type:
Article
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