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PMID: 671194 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

True hermaphroditism: a clinical description and a proposed function for the long arm of the Y chromosome.

Journal of pediatric surgery ·Vol. 13 ·No. 3 ·1978-06-00 ·Pages 293-301

Donahoe PK, Crawford JD, Hendren WH

Abstract

True hermaphroditism is a very rare form of ambiguous genitalia characterized by the presence of both ovarian and testicular tissue in the same individual. Sixty percent of these patients have a 46,XX karyotype; however, most have H-Y antigen detectable. Since H-Y antigen is thought to be the gene product of the short arm of the Y, then the short arm must be present somewhere in the karyotype. Products of the short arm loci are thought to initiate testicular differentiation and male determination. The long arm of the Y has not been detected in true hermaphrodites. Testicular histology in true hermaphrodites is characterized by spermatogenic arrest, causing us to speculate that the long arm of the Y might be essential for germ cell maturation beyond the spermatogonia state.

MeSH Terms
Antigens Disorders of Sex Development/diagnosis,genetics,pathology Female Humans Infant, Newborn Karyotyping Male Mosaicism Ovary/pathology Pregnancy Sex Chromosomes/physiology Sex Determination Analysis Testis/pathology Y Chromosome/physiology
Chemicals
Antigens
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Donahoe P K
Crawford J D
Hendren W H
Article Info
Journal
Journal of pediatric surgery
Abbr.
J Pediatr Surg
ISSN
0022-3468
Published
1978-06-00
Pages
293-301
Language
English
Region
United States
NLM ID
0052631
Subset
IM
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