Presumptive 46,XX-46,XY-47,XXY mosaicism in a hermaphrodite.
نویسندگان
چکیده
منابع مشابه
Chromosome mosaicism in a hermaphrodite.
The chromosome complement in 27 patients with convincing evidence of hermaphroditism has now been investigated. A normal female karyotype (44 autosomes + XX) was reported in I7 cases (Bregman, Bregman, Cushner, and Woods, I963; de Assis, Epps, and Bottura, I960; Dewhurst, Warrack, and Casey, I963; German, Bearn, and McGovern, I962; Gordon, O'Gorman, Dewhurst, and Blank, I960; Harnden and Armstr...
متن کاملPresumptive 46,XX-46,XY-47,XXY mosaicism in a hermaphrodite.
Contrary to the expected XX/XY sex chromosome complements in hermaphroditism, a variety of karyotypes have been reported instead. Dewhurst et al. (1965) summarized from published reports the karyotypic findings in 27 patients with convincing evidence ofhermaphroditism, as follows: 46,XX (17); 46,XY (2); 46,XX/47,XXX (1); 46,XX/46,XX + Frag (1); 46,XX/46,XY (3); 46,XX/47,XXY/ 49,XXYYY (1); 46,XX...
متن کاملJ 7 ournal of Medical Genetics ( 1971 ) . 8 , 117 . Presumptive 46 , XX / 46 , XY / 47 , XXY Mosaicism in a Hermaphrodite AMALA
Contrary to the expected XX/XY sex chromosome complements in hermaphroditism, a variety of karyotypes have been reported instead. Dewhurst et al. (1965) summarized from published reports the karyotypic findings in 27 patients with convincing evidence ofhermaphroditism, as follows: 46,XX (17); 46,XY (2); 46,XX/47,XXX (1); 46,XX/46,XX + Frag (1); 46,XX/46,XY (3); 46,XX/47,XXY/ 49,XXYYY (1); 46,XX...
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متن کاملPrimary infertility in a phenotypic male with 46XX chromosomal constitution.
The case of a 32 year old male with normal male adrenarchal hair pattern, bilateral gynaecomastia, a small phallus, hypospadias and bilateral poorly developed testes presenting with primary infertility secondary to azoospermia and a pelvic cyst is described. Repeated chromosomal analysis showed 46XX chromosomal constitution. Laparotomy revealed a simple cyst between the urinary bladder and the ...
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ژورنال
عنوان ژورنال: Journal of Medical Genetics
سال: 1971
ISSN: 1468-6244
DOI: 10.1136/jmg.8.1.117