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Hurler–Scheie syndrome in Niger: a case series
BACKGROUND: Hurler–Scheie syndrome is an intermediate form of mucopolysaccharidosis type I which is a rare lysosomal storage disorder caused by the deficiency or complete absence of enzyme alpha-L-iduronidase activity. We report the first documented cases of Hurler–Scheie syndrome observed in Niger...
Autores principales: | Assadeck, Hamid, Toudou Daouda, Moussa, Bako, Harouna, Hassane Djibo, Fatimata |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482501/ https://www.ncbi.nlm.nih.gov/pubmed/31018863 http://dx.doi.org/10.1186/s13256-019-2047-2 |
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