A case report of congenital idiopathic hypogonadotropic hypogonadism caused by novel mutation of GNRHR gene

RATIONALE: This study aimed to investigate the genetic mutation characteristics of congenital idiopathic hypogonadotropic hypogonadism (IHH) through the clinical features and genetic analysis of 2 patients with IHH in 1 pedigree. PATIENT CONCERNS: A 23-year-old girl presented with primary amenorrhea...

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Detalles Bibliográficos
Autores principales: Wang, Liping, Lin, Weisheng, Li, Xiaohong, Zhang, Lijuan, Wang, Kai, Cui, Xiaoli, Tang, Shanmei, Fang, Guangguang, Tan, Yan, Wang, Xuelai, Chen, Chuan, Yang, Chuanchun, Tang, Huiru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870162/
https://www.ncbi.nlm.nih.gov/pubmed/33592857
http://dx.doi.org/10.1097/MD.0000000000024007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870162/
https://www.ncbi.nlm.nih.gov/pubmed/33592857
http://dx.doi.org/10.1097/MD.0000000000024007

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