Email this article M.A.Grinberg. - A rare case of malformation: external false duality with congenital absence of the anus. - (Weekly, 1895, No. 23).
- Authors: Kakushkin N.
- Issue: Vol 9, No 9 (1895)
- Pages: 811
- Section: Articles
- URL: https://journals.eco-vector.com/jowd/article/view/46200
- DOI: https://doi.org/10.17816/JOWD99811
- ID: 46200
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Abstract
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.
Full Text
Ребенокъ 8 дней, нареченный женскимъ именемъ, имѣетъ одну только неправильность въ строеніи своего тѣла: большія половыя губы увеличены и содержатъ каждая по продолговатому тѣлу (яички); малыя губы сильно развиты; въ мѣстѣ схожденія ихъ — остроконечное образованіе длиной въ 1 снтм., шириною въ 1/2 снтм., безъ отверстія. На 1/2 снтм. кзади отъ этого образованія имѣется отверстіе съ булавочную головку, выдѣляющее и калъ и мочу. Отверстія задняго прохода на обычномъ мѣстѣ нѣтъ. Авторъ называетъ это уродство: pseudohermophroditismus externus masculinus cum atresia ani vaginalis.
About the authors
N. Kakushkin
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Email: info@eco-vector.com
Russian Federation
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