Literature DB >> 837567

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

A D Chapelle, J Schröder, J Murros, G Tallqvist.   

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:

Year:  1977        PMID: 837567     DOI: 10.1111/j.1399-0004.1977.tb01285.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  20 in total

1.  SRY-negative true hermaphrodites and an XX male in two generations of the same family.

Authors:  E S Ramos; C A Moreira-Filho; Y A Vicente; M A Llorach-Velludo; S Tucci; M H Duarte; A G Araújo; L Martelli
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

2.  Deletion mapping of the testis determining locus with DNA probes in 46,XX males and in 46,XY and 46,X,dic(Y) females.

Authors:  U Müller; T Donlon; M Schmid; N Fitch; C L Richer; M Lalande; S A Latt
Journal:  Nucleic Acids Res       Date:  1986-08-26       Impact factor: 16.971

3.  Heteromorphic X chromosomes in 46,XX males: evidence for the involvement of X-Y interchange.

Authors:  H J Evans; K E Buckton; G Spowart; A D Carothers
Journal:  Hum Genet       Date:  1979-05-23       Impact factor: 4.132

4.  A new case of XX-male (XX/XXY mosaic).

Authors:  P Kaiser; K Gerhard-Ratschow; B Zabel; W Gey
Journal:  Hum Genet       Date:  1977-11-02       Impact factor: 4.132

5.  Heteromorphic X chromosomes in 46,XX males?

Authors:  A de la Chapelle; K Simola; P Simola; S Knuutila; N Gahmberg; L Pajunen; C Lundqvist; S Sarna; J Murros
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132

6.  H-Y antigen-positive male pseudohermaphroditism with 45,X/46,XYq-mosaicism.

Authors:  J B Mailhes; D E Pittaway; J Rary; H Chen; W D Grafton
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

7.  The parental origin of X chromosomes in XX males determined using restriction fragment length polymorphisms.

Authors:  D C Page; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

8.  Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype.

Authors:  R E Magenis; M J Webb; R S McKean; D Tomar; L J Allen; H Kammer; D L Van Dyke; E Lovrien
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

9.  An extended long-range restriction map of the human sex-determining region on Yp, including ZFY, finds marked homology on Xp and no detectable Y sequences in an XX male.

Authors:  V Verga; R P Erickson
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

Review 10.  The human Y chromosome.

Authors:  P Goodfellow; S Darling; J Wolfe
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

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