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

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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Bibliographic Details
Main Authors: Jisun Park, Minjun Jeon, Seri Maeng, Dae Kyu Kwon, Sujin Kim, Ji Eun Lee
Format: Article
Language:English
Published: Korean Society of Pediatric Endocrinology 2022-09-01
Series:Annals of Pediatric Endocrinology & Metabolism
Subjects:
central precocious puberty
hypothalamic hamartomas
microcephaly
seckel syndrome
slipped capital femoral epiphyses
Online Access:http://e-apem.org/upload/pdf/apem-2244066-033.pdf

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http://e-apem.org/upload/pdf/apem-2244066-033.pdf

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