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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

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