Hypogonadotropic hypogonadism associated with another small supernumerary marker chromosome (sSMC) derived from chromosome 22, a case report

The idiopathic hypogonadotropic hypogonadism (IHH) is portrayed as missing or fragmented pubescence, cryptorchidism, small penis, and infertility. Clinically it is characterized by the low level of sex steroids and gonadotropins, normal radiographic findings of the hypothalamic-pituitary areas, and...

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Detalles Bibliográficos
Autores principales: Abdullah, Li, Cui, Zhao, Minggang, Wang, Xiang, Li, Xu, Xing, Junping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100857/
https://www.ncbi.nlm.nih.gov/pubmed/33968667
http://dx.doi.org/10.21037/tau-20-1087

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100857/
https://www.ncbi.nlm.nih.gov/pubmed/33968667
http://dx.doi.org/10.21037/tau-20-1087

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