ロード中...

A Case of Turner Syndrome with Concomitant Transient Hypogammaglobulinaemia of Infancy and Central Diabetes Insipidus

Turner syndrome (TS) is a genetic disorder that affects development in females and is characterized by the complete or partial absence of the second sex chromosome, or monosomy X. TS is associated with abnormalities in lymphatic and skeletal development, in growth, and in gonadal function. Cardiac a...

詳細記述

保存先:
書誌詳細
主要な著者: Korkmaz, Hüseyin Anıl, Özkan, Behzat, Hazan, Filiz, Büyükinan, Muammer, Çelik, Tanju
フォーマット: Artigo
言語:Inglês
出版事項: Galenos Publishing 2013
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3628396/
https://ncbi.nlm.nih.gov/pubmed/23419422
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/Jcrpe.880
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!