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
Hauptverfasser: van Gelderen, H. H., Opitz, John M.
Format: Artikel
Sprache:eng
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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.
ISSN:0148-7299
1096-8628
DOI:10.1002/ajmg.1320130406