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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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Detalles Bibliográficos
Autores principales:	Belli, Gilda, Bartolini, Emanuele, Bianchi, Andrea, Mascalchi, Mario, Stagi, Stefano
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2018
Materias:	Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117375/ https://www.ncbi.nlm.nih.gov/pubmed/30197627 http://dx.doi.org/10.3389/fendo.2018.00497

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