Syndrome of total alopecia, multiple skeletal anomalies, shortness of stature, and mental deficiency
This is a report of a 16‐year‐old boy with mental deficiency, shortness of stature, peculiar face and skull, multiple skeletal anomalies, limb contractures, total alopecia, and probable hypothalamic hypogonadism. A striking resemblance exists between this case and a female adolescent described in 19...
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Veröffentlicht in: | American journal of medical genetics 1982-12, Vol.13 (4), p.383-387 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | This is a report of a 16‐year‐old boy with mental deficiency, shortness of stature, peculiar face and skull, multiple skeletal anomalies, limb contractures, total alopecia, and probable hypothalamic hypogonadism. A striking resemblance exists between this case and a female adolescent described in 1980 by Schinzel. It is suggested that these two cases represent a previously unrecognized syndrome. The fact that this boy was born from a first‐cousin marriage suggests autosomal recessive inheritance. |
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ISSN: | 0148-7299 1096-8628 |
DOI: | 10.1002/ajmg.1320130406 |