| Literature DB >> 30560013 |
Xiaoxiao Cui1,2, Yazhou Cui2, Liang Shi2, Jing Luan2, Xiaoyan Zhou2, Jinxiang Han2.
Abstract
Turner syndrome (TS), also known as Congenital ovarian hypoplasia syndrome, occurs when the X chromosome is partially or completely missing in females. Its main clinical manifestations include growth disorders, reproductive system abnormalities, cardiovascular abnormalities, and autoimmune diseases. TS is highly prevalent in China. Timely diagnosis is crucial, and non-invasive prenatal DNA testing can identify TS and other diseases. Treatment of TS mainly involves administration of growth hormone combined with very low doses of estrogen to increase the patients height. This article describes the incidence, complications, diagnosis, and treatment of TS.Entities:
Keywords: Turner syndrome; clinical features; complication; diagnosis; treatment
Year: 2018 PMID: 30560013 PMCID: PMC6290843 DOI: 10.5582/irdr.2017.01056
Source DB: PubMed Journal: Intractable Rare Dis Res ISSN: 2186-3644