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...

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Detalles Bibliográficos
Autores principales: Milazzo, Jean-Pierre, Bironneau, Amandine, Vannier, Jean-Pierre, Liard-Zmuda, Agnes, Macé, Bertrand, Nathalie, Rives
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
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

Internet

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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