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Chediak–Higashi Syndrome Presented as Accelerated Phase: Case Report and Review of the Literature
Chediak–Higashi syndrome (CHS) is a rare autosomal recessive disease, characterized by partial oculocutaneous albinism, recurrent pyogenic infections (skin, mucosa and respiratory system), and neurologic deficit. The hallmark of this syndrome is the presence of abnormal intracytoplasmic giant granul...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer India
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4192156/ https://ncbi.nlm.nih.gov/pubmed/25332584 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-014-0336-x |
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