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...

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Bibliographic Details
Published in:	Frontiers in Endocrinology
Main Authors:	Gilda Belli, Emanuele Bartolini, Andrea Bianchi, Mario Mascalchi, Stefano Stagi
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2018-08-01
Subjects:	metachromatic leucodystrophy central precocious puberty precocious puberty metabolic disease white matter disease
Online Access:	https://www.frontiersin.org/article/10.3389/fendo.2018.00497/full

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