M.A.Grinberg. - A rare case of malformation: external false duality with congenital absence of the anus. - (Weekly, 1895, No. 23).
- 作者: Kakushkin N.
- 期: 卷 9, 编号 9 (1895)
- 页面: 811
- 栏目: Articles
- URL: https://medbiosci.ru/jowd/article/view/46200
- DOI: https://doi.org/10.17816/JOWD99811
- ID: 46200
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A child of 8 days, named by a woman's name, has only one irregularity in the structure of his body: the labia majora are enlarged and each contain an oblong body (testicles); small lips strongly developed; in the place of similarity of them - a pointed formation with a length of 1 cm., a width of 1/2 cm., without a hole. 1/2 sntm. posterior to this formation there is an opening with a pinhead, which expels both feces and urine. The holes of the anus in the usual place are nѣt. The author calls this deformity: pseudohermophroditismus externus masculinus cum atresia ani vaginalis.
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