Abstract
This is a study of 3 cases of the Laurence-Moon-Bardet-Biedl syndrome in two families. In one family the parents were consaguineous (first cousins). The authors studied the main symptoms and insist on the importance of the ophthalmological manifestation. No hypophyseal involvement was observed in these cases.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adolescent
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Child
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Chromosome Aberrations
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Female
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Fingers / abnormalities
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Humans
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Hypogonadism / complications
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Laurence-Moon Syndrome / classification
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Laurence-Moon Syndrome / complications*
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Laurence-Moon Syndrome / genetics
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Laurence-Moon Syndrome / pathology
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Male
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Mental Disorders / complications
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Obesity / complications
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Retinal Diseases / complications
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Toes / abnormalities