Two Sisters with Kallmann Syndrome, Gonadal Dysgenesis, and Multiple Neuromuscular and Endocrine Disorders: Report of Two Cases with Description of an Unusual Association

Kallmann syndrome (KS) is an uncommon genetic disorder characterized by isolated congenital hypogonadotropic hypogonadism (CHH) and anosmia/hyposmia. KS originates from abnormal embryonic migration of olfactory axons and gonadotropin-releasing hormone (GnRH)-synthesizing neurons. It can be challengi...

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Detalles Bibliográficos
Autores principales: Camacho, Marta, Castelo-Branco, Camil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Reproductive Endocrinology: Case Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537203/
https://www.ncbi.nlm.nih.gov/pubmed/35199317
http://dx.doi.org/10.1007/s43032-022-00897-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537203/
https://www.ncbi.nlm.nih.gov/pubmed/35199317
http://dx.doi.org/10.1007/s43032-022-00897-z

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