Familial Leydig Cell Hypoplasia as a Cause of Male Pseudohermaphroditism

A case of familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism is described in two 46,XY female sibs. Biochemical and histologic evidence for such diagnosis is presented.

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Bibliographische Detailangaben
Veröffentlicht in:	Human heredity 1987-01, Vol.37 (1), p.36-40
Hauptverfasser:	El-Awady, Mostafa K., Temtamy, Samia A., Salam, Moushira A., Gad, Yehia Z.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Disorders of Sex Development - genetics Genotype Gynecology. Andrology. Obstetrics Hormones - blood Humans Leydig Cells - pathology Male Male and female genital diseases. Gonadal dysgenesis. Hermaphroditism. Sex hormones resistance Medical sciences Original Paper Original Papers Pedigree Receptors, Androgen - physiology Testicular Diseases - genetics Testicular Diseases - pathology Testis - pathology
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