Literature DB >> 9135271

Presence of Turner stigmata in a case of dysgenetic male pseudohermaphroditism with 45,X/46,X+mar karyotype.

H Hashimoto1, H Maruyama, R Koshida, N Okuda, K Murayama, T Katsumi, K Watanabe, T Sato.   

Abstract

A case is reported of dysgenetic male pseudohermaphroditism (DMPH) having Turner stigmata and 45,X/46,X+mar karyotype. The marker chromosome of this patient consisted of most if not all of the short arm, including the sex determining region of the Y chromosome. Although this karyotype is relatively common in Turner's syndrome and occasionally observed in mixed gonadal dysgenesis, DMPH is usually exemplified by a 46,XY karyotype except for one patient reported with 45,X/46,XY mosaicism. Turner stigmata have not previously been reported in DMPH. The present patient is an intermediate case between mixed gonodal dysgenesis and typical DMPH, and this indicates that 45,X/ 46,X +mar karyotype abnormality can result in a wide range of phenotype such as DMPH, mixed gonodal dysgenesis and Turner's syndrome.

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Year:  1997        PMID: 9135271      PMCID: PMC1717119          DOI: 10.1136/adc.76.3.268

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  11 in total

1.  The majority of the marker chromosomes in Japanese patients with stigmata of Turner syndrome are derived from Y chromosomes.

Authors:  S Nagafuchi; T Tamura; Y Nakahori; K Takano; Y Nishi; N Iwatani; M Kitao; Y Hori; S Konda; T Hasegawa
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

2.  Clinical and endocrine spectrum in patients with the 45,X/46,XY karyotype.

Authors:  S Kofman; G Pérez-Palacios; M Medina; N Escobar; M García; L Ruz; O Mutchinick; R Lisker
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 3.  Chromosomal localisation of a gene(s) for Turner stigmata on Yp.

Authors:  T Ogata; C Tyler-Smith; S Purvis-Smith; G Turner
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

4.  Dysgenetic male pseudohermaphroditism.

Authors:  J Rajfer; G Mendelsohn; J Arnheim; R D Jeffs; P C Walsh
Journal:  J Urol       Date:  1978-04       Impact factor: 7.450

5.  Clinical and pathologic spectrum of 46,XY gonadal dysgenesis: its relevance to the understanding of sex differentiation.

Authors:  G D Berkovitz; P Y Fechner; H W Zacur; J A Rock; H M Snyder; C J Migeon; E J Perlman
Journal:  Medicine (Baltimore)       Date:  1991-11       Impact factor: 1.889

6.  Chromosomal localisation of a pseudoautosomal growth gene(s).

Authors:  T Ogata; C Petit; G Rappold; N Matsuo; T Matsumoto; P Goodfellow
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

7.  Mixed gonadal dysgenesis and dysgenetic male pseudohermaphroditism--a critical analysis.

Authors:  M Rohatgi; D K Gupta; P S Menon; I C Verma; M Mathur
Journal:  Indian J Pediatr       Date:  1992 Jul-Aug       Impact factor: 1.967

Review 8.  A case of mixed gonadal dysgenesis (MGD)--with a review of MGD patients reported in Japan.

Authors:  N Yamakita; K Yasuda; H Mori; M Kuriyama; Y Kumamoto; K Miura
Journal:  Jpn J Med       Date:  1989 Nov-Dec

9.  The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.

Authors:  E Therman; B Susman
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

10.  A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif.

Authors:  A H Sinclair; P Berta; M S Palmer; J R Hawkins; B L Griffiths; M J Smith; J W Foster; A M Frischauf; R Lovell-Badge; P N Goodfellow
Journal:  Nature       Date:  1990-07-19       Impact factor: 49.962

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  1 in total

1.  Description of children with 45,X/46,XY karyotype.

Authors:  Hanan Tosson; Susan R Rose; Lou Ann Gartner
Journal:  Eur J Pediatr       Date:  2011-10-14       Impact factor: 3.183

  1 in total

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