Chinese familial central precocious puberty with hyperuricemia due to recurrent DLK1 mutation: Case report and review of the literature

Chinese familial central precocious puberty with hyperuricemia due to recurrent DLK1 mutation: Case report and review of the literature

Abstract Background Central precocious puberty (CPP) is a precocious puberty due to premature activation of the hypothalamic–pituitary‐gonadal axis (HPG). MKRN3 defects are well‐known causes of CPP, while DLK1 mutations were recently identified in a few patients with CPP. Methods The study was appro...

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Bibliographic Details
Main Authors: Gaopin Yuan, Xiaohong Zhang, Shaofeng Liu, Tingli Chen
Format: Article
Language:English
Published: Wiley 2022-12-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
central precocious puberty
DLK1
hyperuricemia
maternal imprinting
Online Access:https://doi.org/10.1002/mgg3.2087

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