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

Internet

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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