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Mucopolysaccharidosis Type I and Bilateral Optic Disc Edema
Mucopolysaccharidosis type I (MPS I or Hurler syndrome) is a multisystem genetic disorder caused by α-L-iduronidase (IDUA) deficiency, which leads to widespread accumulation of glycosaminoglycans triggering tissue damage and organ dysfunction. A variety of ocular manifestations have been described i...
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| Publicado no: | Neuroophthalmology |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7053928/ https://ncbi.nlm.nih.gov/pubmed/32165899 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/01658107.2018.1520903 |
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