THU201 Atypical Presentation Of Kallmann Syndrome With A Rare Genetic Mutation

Disclosure: E.L. Montgomery: None. B. Thrasher: None. S. Watson: None. Kallmann Syndrome presents as idiopathic hypogonadotropic hypogonadism with additional findings of hyposmia or anosmia and midline facial defects, including cleft lip/palate. We present a case of Kallmann Syndrome due to a rare g...

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Detalles Bibliográficos
Autores principales: Montgomery, Emily L, Thrasher, Bradly, Watson, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554227/
http://dx.doi.org/10.1210/jendso/bvad114.1452

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554227/
http://dx.doi.org/10.1210/jendso/bvad114.1452

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