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hrp0098p1-86 | Pituitary, Neuroendocrinology and Puberty 1 | ESPE2024

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

Kagami Masayo , Narusawa Hiromune , Ogawa Tomoe , Yagasaki Hideaki , Nagasaki Keisuke , Urakawa Tatsuki , Saito Tomohiro , Soneda Shun , Sano Shinichiro , Mamada Mitsukazu , Terashita Shintaro , Dateki Sumito , Narumi Satoshi , Naiki Yasuhiro , Horikawa Reiko , Ogata Tsutomu

Background: Defects of MKRN3, DLK1, KISS1, and KISS1R and some disorders, such as Temple syndrome (TS14), cause central precocious puberty (CPP). Furthermore, MECP2 was reported as a causative gene for CPP in 2023. To our knowledge, comprehensive studies on (epi)genetic abnormalities, clinical features, and hormonal features in patients with CPP have not been reported.Methods: In 90 CP...

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

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