Comprehensive study on central precocious puberty: molecular and clinical analyses in 90 patients

Hiromune Narusawa; Tomoe Ogawa; Hideaki Yagasaki; Keisuke Nagasaki; Tatsuki Urakawa; Tomohiro Saito; Shun Soneda; Saori Kinjo; Shin‐ichiro Sano; Mitsukazu Mamada; Shintaro Terashita; Sumito Dateki; Satoshi Narumi; Yasuhiro Naiki; Reiko Horikawa; Tsutomu Ogata; Maki Fukami; Masayo Kagami

doi:10.1210/clinem/dgae666

Abstract

Defects in MKRN3, DLK1, KISS1, and KISS1R and some disorders, such as Temple syndrome (TS14), cause central precocious puberty (CPP). Recently, pathogenic variants (PVs) in MECP2 have been reported to be associated with CPP.

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Narusawa et al. (2024) studied this question.

synapsesocial.com/papers/68e57432b6db643587514542 https://doi.org/10.1210/clinem/dgae666

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Comprehensive study on central precocious puberty: molecular and clinical analyses in 90 patients

Abstract

Discussion

Cite This Study

Comprehensive study on central precocious puberty: molecular and clinical analyses in 90 patients

Abstract

Discussion

Cite This Study

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