Najjar syndrome revisited

We describe 2 brothers with cardiomyopathy and hypergonadotropic hypogonadism and conclude that this is the first description of the Najjar syndrome in the United States. The inheritance may be autosomal recessive. © 1993 Wiley‐Liss, Inc.

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Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics 1993-12, Vol.47 (8), p.1151-1152
Hauptverfasser:	Thomas, I. T., Jewett, T., Lantz, P., Covitz, W., Garber, P., Berry, M. N.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Cardiomyopathies - genetics cardiomyopathy case reports Complex syndromes genital anomaly gonads Humans hypergonadotropic hypogonadism Hypogonadism - genetics Infant, Newborn inheritance Male man Medical genetics Medical sciences Najjar syndrome Najjar's syndrome Syndrome
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Beschreibung
Zusammenfassung:	We describe 2 brothers with cardiomyopathy and hypergonadotropic hypogonadism and conclude that this is the first description of the Najjar syndrome in the United States. The inheritance may be autosomal recessive. © 1993 Wiley‐Liss, Inc.
ISSN:	0148-7299 1096-8628
DOI:	10.1002/ajmg.1320470803