A rare disease of Kallmann syndrome: A case report

Kallmann syndrome (KS) is a rare genetic disorder that refers to the association between hypogonadotropic hypogonadism and anosmia or hyposmia due to abnormal migration of olfactory axons and gonadotropin-releasing hormone-producing neurons. Here, we present a case of a 40-year-old man who presented...

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Detalles Bibliográficos
Autores principales: Hilman, Syawaluddin, Dewi, Dian Komala, Kartika, Euis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842794/
https://www.ncbi.nlm.nih.gov/pubmed/36660569
http://dx.doi.org/10.1016/j.radcr.2022.12.036

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842794/
https://www.ncbi.nlm.nih.gov/pubmed/36660569
http://dx.doi.org/10.1016/j.radcr.2022.12.036

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