Le syndrome de Kallmann-de Morsier: à propos de trois cas

Kallmann-de Morsier syndrome (KS) is a genetic disease of the olfactory system characterized by the association of hypogonadotropic hypogonadism also referred to as gonadotropin-releasing hormone (GnRH) deficiency and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs). Apart fro...

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Detalles Bibliográficos
Autores principales: Marhari, Halima, Chahdi Ouazzani, Fatima Zahra, Ouahabi, Hanan El, Bouguenouch, Laila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814956/
https://www.ncbi.nlm.nih.gov/pubmed/31692807
http://dx.doi.org/10.11604/pamj.2019.33.221.11678

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814956/
https://www.ncbi.nlm.nih.gov/pubmed/31692807
http://dx.doi.org/10.11604/pamj.2019.33.221.11678

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