Central precocious puberty with hypothalamic hamartoma: the first case reports of 2 siblings with different phenotypes of Seckel syndrome 5

Hypothalamic hamartomas (HHs) are nonneoplastic mass lesions located in the hypothalamus that can cause central precocious puberty (CPP) and/or gelastic seizures. Seckel syndrome 5 (OMIM210600, SCKL5) is a rare autosomal recessive genetic spectrum disorder characterized by intrauterine growth retard...

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Detalles Bibliográficos
Autores principales: Park, Jisun, Jeon, Minjun, Maeng, Seri, Kwon, Dae Kyu, Kim, Sujin, Lee, Ji Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556446/
https://www.ncbi.nlm.nih.gov/pubmed/35798296
http://dx.doi.org/10.6065/apem.2244066.033

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