Familial true hermaphrodism in three siblings: clinical, cytogenetic, histological and hormonal studies

Three affected siblings with the hermaphrodism are described. The propositi showed the following characteristics: male phenotype and gender role, hypospadias, bilateral scrotal ovotestes with palpable nodules, and absence of müllerian structures. The X chromatin was positive and the Y chromatin was...

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Bibliographic Details
Published in:	Humangenetik Vol. 29; no. 2; p. 99
Main Authors:	Armendares, S, Salamanca, F, Cantú, J M, Del Castillo, V, Nava, S, Dominguez-de-la-Piedra, E, Cortés-Gallegos, V, Gallegos, A, Cervantes, C, Parra, A
Format:	Journal Article
Language:	English
Published:	Germany 10.09.1975
Subjects:	Adolescent Breast - pathology Child Disorders of Sex Development - blood Disorders of Sex Development - genetics Disorders of Sex Development - pathology Estradiol - blood Female Follicle Stimulating Hormone - blood Genitalia - abnormalities Humans Leydig Cells - pathology Luteinizing Hormone - blood Male Menstruation Ovary - pathology Pedigree Phenotype Progesterone - blood Sex Chromatin - analysis Testis - pathology Testosterone - blood
ISSN:	0018-7348
Online Access:	Get more information
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