首页> 美国卫生研究院文献>Archives of Disease in Childhood >Presence of Turner stigmata in a case of dysgenetic malepseudohermaphroditism with 45X/46X+mar karyotype
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Presence of Turner stigmata in a case of dysgenetic malepseudohermaphroditism with 45X/46X+mar karyotype

机译:男性发育不全的情况下特纳柱头的存在具有45X / 46X + mar核型的假雌雄同体

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摘要

Accepted 19 November 1996
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.

机译:1996年11月19日被接受。
报道了一例具有特纳柱头和45,X / 46,X + mar核型的不遗传的雄性假性雌性双性生殖器(DMPH)。该患者的标记染色体由大部分(如果不是全部)短臂组成,包括Y染色体的性别决定区域。尽管这种核型在特纳综合征中相对常见,偶尔在混合性腺发育不全中观察到,但DMPH通常以46,XY核型为例,除了一位报道有45,X / 46,XY镶嵌症的患者。 DMPH中以前没有报道过Turner stigmata。本例患者是混合型性腺发育不全和典型的DMPH之间的中间病例,这表明45,X / 46,X + mar核型异常可导致多种表型,例如DMPH,混合性性腺发育不全和特纳氏综合症。 br />

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