Clinical characteristics and follow-up of 5 young Chinese males with gonadotropin-releasing hormone deficiency caused by mutations in the KAL1 gene

Isolated gonadotropin-releasing hormone (GnRH) deficiency (IGD) pertains to a group of genetic disorders consisting of anosmic hypogonadotropic hypogonadism (Kallmann syndrome, KS) and normosmic idiopathic hypogonadotropic hypogonadism (nIHH). KS is genetically heterogeneous. We hereby present 5 you...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Juan, Li, Niu, Ding, Yu, Huang, Xiaodong, Shen, Yongnian, Wang, Jian, Wang, Xiumin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707242/
https://www.ncbi.nlm.nih.gov/pubmed/26862482
http://dx.doi.org/10.1016/j.mgene.2015.12.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707242/
https://www.ncbi.nlm.nih.gov/pubmed/26862482
http://dx.doi.org/10.1016/j.mgene.2015.12.001

Ejemplares similares