Suppr超能文献

先天性皮肤发育不全与母亲甲状腺疾病治疗的关联。

The association of aplasia cutis congenita with therapy of maternal thyroid disease.

作者信息

Kalb R E, Grossman M E

出版信息

Pediatr Dermatol. 1986 Sep;3(4):327-30. doi: 10.1111/j.1525-1470.1986.tb00534.x.

Abstract

Aplasia cutis congenita, the localized absence of skin at birth, usually is an isolated scalp defect. We examined an infant with aplasia cutis congenita associated with maternal Grave's disease and the use of methimazole during pregnancy. This association was reported twice before. It has certain implications with respect to therapy of pregnant hyperthyroid women.

摘要

先天性皮肤发育不全,即出生时局部皮肤缺失,通常表现为孤立的头皮缺损。我们检查了一名患有先天性皮肤发育不全的婴儿,其与母亲的格雷夫斯病以及孕期使用甲巯咪唑有关。此前曾有两次关于这种关联的报道。这对于妊娠甲亢妇女的治疗具有一定意义。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验