Congenital hypopituitarism in familial Turner syndrome cases caused by a highly prevalent PROP1 gene mutation in Tunisia

Background: Turner syndrome (TS) is a genetic disorder found only in females who are completely or partially missing an X chromosome. It is rarely inherited from parent to offspring and is not reported to be associated with any causal gene. In addition, familial forms are less frequent than sporadic...

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出版年:	Endocrine and Metabolic Science
主要な著者:	Hassen Hadj Kacem, Mariam Moalla, Faten Hadj Kacem, Oumeyma Trimeche, Wajdi Safi, Mouna Mnif-Feki, Mohamed Abid
フォーマット:	論文
言語:	英語
出版事項:	Elsevier 2024-03-01
主題:	Turner syndrome Congenital hypopituitarism PROP1 gene
オンライン･アクセス:	http://www.sciencedirect.com/science/article/pii/S2666396124000049