Suppr超能文献

具有家族性模式的头皮先天性皮肤发育不全

Aplasia Cutis Congenita of the Scalp with a Familial Pattern.

作者信息

AlShehri Waleed, AlFadil Sara, AlOthri Alhanouf, Alabdulkarim Abdulaziz O, Wani Shabeer A, Rabah Sari M

机构信息

Department of Plastic & Reconstructive Surgery, King Fahad Medical City, Riyadh 11525, Saudi Arabia.

出版信息

Case Rep Surg. 2016;2016:4264721. doi: 10.1155/2016/4264721. Epub 2016 Jun 26.

Abstract

Aplasia Cutis Congenita (ACC) is a condition characterized by congenital absence of skin, usually on the scalp. ACC can occur as an isolated condition or in the presence of other congenital anomalies. Here we describe a case of a 16-day-old baby girl with an isolated ACC of the scalp. Her elder two siblings have been diagnosed with ACC with concomitant cardiac or limb anomalies. The patient was managed conservatively until the defect has formed scar tissue 6 months later.

摘要

先天性皮肤发育不全(ACC)是一种以先天性皮肤缺失为特征的疾病,通常发生在头皮上。ACC可作为一种孤立的病症出现,也可伴有其他先天性异常。在此,我们描述一例16天大的女婴,其头皮患有孤立性ACC。她的两个哥哥已被诊断患有ACC并伴有心脏或肢体异常。该患者接受了保守治疗,直到6个月后缺损形成瘢痕组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1a5/4939192/1522b4174e73/CRIS2016-4264721.001.jpg

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