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

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...

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Veröffentlicht in:Archives of disease in childhood 1997-03, Vol.76 (3), p.268-271
Hauptverfasser: Hashimoto, Hiroyuki, Maruyama, Hiroaki, Koshida, Rie, Okuda, Norihiko, Murayama, Kazuo, Katsumi, Tetsuro, Watanabe, Kishichiro, Sato, Tamotsu
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Sprache:eng
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Zusammenfassung: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.
ISSN:0003-9888
1468-2044
DOI:10.1136/adc.76.3.268