Central Precocious Puberty in a Child With Metachromatic Leukodystrophy

Metachromatic leucodystrophy (MLD) is a rare inherited lysosomal disorder caused by reduced activity of the enzyme arylsulfatase A with accumulation of sulfatides in the nervous system. We report a female child affected by MLD who developed central precocious puberty (CPP). This association has not...

詳細記述

書誌詳細

出版年:	Frontiers in Endocrinology
主要な著者:	Gilda Belli, Emanuele Bartolini, Andrea Bianchi, Mario Mascalchi, Stefano Stagi
フォーマット:	論文
言語:	英語
出版事項:	Frontiers Media S.A. 2018-08-01
主題:	metachromatic leucodystrophy central precocious puberty precocious puberty metabolic disease white matter disease
オンライン･アクセス:	https://www.frontiersin.org/article/10.3389/fendo.2018.00497/full