Suppr超能文献

遗传性单纯性头皮毛发稀少症

Hereditary hypotrichosis simplex of the scalp.

作者信息

Moravvej-Farshi Hamideh, Ayatollahi Azin, Hejazi Somayeh

机构信息

Department of Dermatology, Skin Research Center, Shahid Beheshti University of Medical Sciences, Shohada-e Tajrish Hospital, Tehran, Iran.

出版信息

Indian J Dermatol. 2014 Nov;59(6):634. doi: 10.4103/0019-5154.143586.

Abstract

Hereditary hypotrichosis simplex of the scalp is a genetic disorder, characterized by sparse or absent scalp hair without structural defects, in the absence of other ectodermal or systemic abnormalities. Structural hair defects may be presented with a genetic disorder affecting hair growth or part of a congenital syndrome or may indicate underlying metabolic disorders, or may be associated with other diseases. We describe a 26-years-old Persian girl suffering from hypotrichosis simplex of the scalp with trichorrhexis nodosa who had no ectodermal defects and systemic disease.

摘要

遗传性单纯性头皮毛发稀少症是一种遗传性疾病,其特征是头皮毛发稀疏或缺失且无结构缺陷,同时不存在其他外胚层或全身性异常。结构性毛发缺陷可能与影响头发生长的遗传性疾病、先天性综合征的一部分有关,也可能表明存在潜在的代谢紊乱,或者与其他疾病相关。我们描述了一名26岁的波斯女孩,她患有伴有结节性脆发症的单纯性头皮毛发稀少症,且无外胚层缺陷和全身性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9ed/4248538/0729953002bb/IJD-59-634b-g001.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