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Precocious initiation of spermatogenesis in a 19-month-old boy with Hurler syndrome
Mucopolysaccharidosis type IH (MPS IH) is a rare autosomal recessive lysosomal storage disorder. Haematopoietic stem cell transplantation (HSCT) has been proposed for the treatment of MPS IH patients and offers the possibility to grow into their adulthood. Precocious puberty has been described in fe...
Autores principales: | Milazzo, Jean-Pierre, Bironneau, Amandine, Vannier, Jean-Pierre, Liard-Zmuda, Agnes, Macé, Bertrand, Nathalie, Rives |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349721/ https://www.ncbi.nlm.nih.gov/pubmed/25780582 http://dx.doi.org/10.1186/2051-4190-24-8 |
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