Dizygotic twin sisters with normosmic idiopathic hypogonadotropic hypogonadism caused by an FGFR1 gene variant

Isolated hypogonadotropic hypogonadism (IHH) is a rare genetic disorder that is clinically and genetically heterogeneous. It is characterized by absent or incomplete pubertal development owing to an isolated defect in the production, secretion, or action of gonadotropin-releasing hormone. The incide...

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Detalles Bibliográficos
Autores principales: Choe, Jaewon, Kim, Jae Hyun, Kim, Young Ah, Lee, Jieun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538301/
https://www.ncbi.nlm.nih.gov/pubmed/32871658
http://dx.doi.org/10.6065/apem.1938148.074

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538301/
https://www.ncbi.nlm.nih.gov/pubmed/32871658
http://dx.doi.org/10.6065/apem.1938148.074

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