特纳氏综合症
Also known as Bonnevie-Ullrich syndrome, Bonnevie-Ullrich syndrome NOS, Bonnevie-Ullrich syndrome NOS (disorder), Gonadal dysgenesis - Turner, Karyotype 45, X, Monosomy X, Turner syndrome (disorder), Turner's syndrome NOS
chromosomal variation where a person is born with a 45X chromosome pattern rather than the typical 46XX
AI overview
Turner syndrome is a genetic condition where a person is born with one X chromosome instead of the typical two sex chromosomes. This chromosomal difference can affect physical development and health in various ways throughout a person's life.
AI-generated from the Wikipedia summary — may contain errors.
Research
13,146 papers- Turner Syndrome: An Update.ReviewAdvances in pediatrics · 2022Steiner M, Saenger PDOI: 10.1016/j.yapd.2022.03.004
- Turner syndrome.ReviewChild and adolescent psychiatric clinics of North America · 2007Kesler SRDOI: 10.1016/j.chc.2007.02.004
- Turner's syndrome.ReviewLancet (London, England) · 2001Ranke MB, Saenger PDOI: 10.1016/S0140-6736(01)05487-3
- Turner syndrome.ReviewPediatrics in review · 2013Milbrandt T, Thomas EDOI: 10.1542/pir.34-9-420
Article · 中文
透納氏症（英語：Turner syndrome，縮寫：TS），或稱45,X、45,X0，為的一種，是雌性個體因X染色體部分或完全缺失而引發的疾病。透納氏症患者的症狀各異，患者常常會有短而成、、頸後髮際線較低、矮小，出生時即手腳水腫等特徵。一般來說，透納氏症患者沒有月經、乳房不發育而且不孕，且患有先天性心臟病、糖尿病以及甲狀腺功能低下症的機率較正常人高。大部分的透納氏症患者的智力水平正常，但許多患者的低下，比如學習數學所需要的。透納氏症患者有視覺和聽覺障礙的機率也較正常人高。
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