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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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Detalhes bibliográficos
Principais autores: Bouatay, Amina, Hizem, Sondes, Tej, Amel, Moatamri, Wided, Boughamoura, Lamia, Kortas, Mondher
Formato: Artigo
Idioma:Inglês
Publicado em: Springer India 2014
Assuntos:
Acesso em linha: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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