An Indian Boy with Griscelli Syndrome Type 2: Case Report and Review of Literature

Griscelli syndrome 2 is a rare autosomal recessive disorder of pigmentary dilution of hair, skin, splenohepatomegaly, pancytopenia, immune and neurologic dysfunction. Clinical course is characterized by recurrent infection triggered by uncontrolled T-lymphocyte and macrophage activation, called hemo...

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Detalles Bibliográficos
Autores principales: Singh, Ankur, Garg, Amit, Kapoor, Seema, Khurana, Nita, Entesarian, Miriam, Tesi, Bianca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103279/
https://www.ncbi.nlm.nih.gov/pubmed/25071262
http://dx.doi.org/10.4103/0019-5154.135494

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103279/
https://www.ncbi.nlm.nih.gov/pubmed/25071262
http://dx.doi.org/10.4103/0019-5154.135494

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