Idiopathic hypogonadotropic hypogonadism caused by compound heterozygosity for two novel mutations in the GNRH1 gene: a case report

BACKGROUND: Idiopathic hypogonadotropic hypogonadism (IHH) is a rare congenital or acquired genetic disorder caused by gonadotropin-releasing hormone (GnRH) deficiency. IHH patients are divided into two major groups, hyposmic or anosmic IHH (Kallmann syndrome) and normosmic IHH (nIHH), according to...

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Detalles Bibliográficos
Autores principales: Tian, Qingqing, Tang, Jingjing, Wang, Lihong, Liu, Jiaojiao, Li, Xiangshan, Cao, Zhuozhuo, Tian, Zhufang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557371/
https://www.ncbi.nlm.nih.gov/pubmed/37798680
http://dx.doi.org/10.1186/s12902-023-01455-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557371/
https://www.ncbi.nlm.nih.gov/pubmed/37798680
http://dx.doi.org/10.1186/s12902-023-01455-7

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