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PMID: 837567 Published · ppublish English Case Reports Journal Article

Two XX males in one family and additional observations bearing on the etiology of XX males.

Clinical genetics ·Vol. 11 ·No. 2 ·1977-02-00 ·Pages 91-106

Chapelle AD, Schröder J, Murros J, Tallqvist G

Abstract

Two XX males who were second cousins are reported. A genetic mechanism producing maleness is suggested. The putative factor had been transmitted solely through males, which excludes the possibility of a heritable X-Y interchange. Recent reports on fluorescent Y chromatin in Sertoli cells of XX males prompted investigations into the fluorescence patterns of testicular cells. Sertoli cells from three XX males displayed brightly fluorescent spots, but it was concluded that they did not represent Y chromosomes. Evidence for this conclusion was obtained from the study of testicular fluorescence in XX, XXY and XY males. No visually detectalbe cytogenetic evidence for an increase in length or altered banding pattern of one of the X chromosomes was found in three XX males. We conclude that an autosomal gene is the most likely explanation of the male differentiation in the two XX males presented here.

MeSH Terms
Adolescent Adult Gynecomastia Humans Male Mitosis Mosaicism Pedigree Sex Chromatin Sex Chromosome Aberrations/genetics Sex Chromosomes Testis/ultrastructure Translocation, Genetic
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Chapelle A D
Schröder J
Murros J
Tallqvist G
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1977-02-00
Pages
91-106
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
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