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

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 approved by...

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Detalles Bibliográficos
Autores principales: Yuan, Gaopin, Zhang, Xiaohong, Liu, Shaofeng, Chen, Tingli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747546/
https://www.ncbi.nlm.nih.gov/pubmed/36353763
http://dx.doi.org/10.1002/mgg3.2087

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747546/
https://www.ncbi.nlm.nih.gov/pubmed/36353763
http://dx.doi.org/10.1002/mgg3.2087

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