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先天性皮肤发育不全

[Aplasia cutis congenita].

作者信息

Trevizo Ortiz L, Ruiz-Maldonado R, Tamayo s L

出版信息

Bol Med Hosp Infant Mex. 1978 Mar-Apr;35(2):333-42.

PMID:626656
Abstract

Communication of fifteen cases of Aplasia Cutis Congenita, seen from 1971 to 1977, in the Department of Pediatric Dermatology at the Hospital del Niño DIF (formerly IMAN). Patients of both sexes were equally affected. The scalp was by far the most common location of lesions. Lesiones were usually single and when multiple, they were symmetrical. The family history for the disease was negative. No relationship could be found with obstetric trauma or with the number of pregnancies. Epithelialized lesions were present in fourteen cases and ulcerated lesions in one. The more frequent congenital associated malformations were: cutaneous, neurological, ocular and osseous.

摘要

1971年至1977年期间,在国家儿童综合发展系统医院(原墨西哥营养研究所)儿科皮肤科诊治的15例先天性皮肤发育不全病例报告。男女患者受影响程度相同。头皮是迄今为止最常见的病变部位。病变通常为单发,若为多发则呈对称性分布。家族病史呈阴性,未发现与产科创伤或妊娠次数有关。14例为上皮化病变,1例为溃疡病变。较常见的先天性相关畸形有:皮肤、神经、眼部和骨骼方面的畸形。

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