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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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| Pubblicato in: | Front Endocrinol (Lausanne) |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6117375/ https://ncbi.nlm.nih.gov/pubmed/30197627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2018.00497 |
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