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Griscelli syndrome type-3

Griscelli syndrome (GS) is a rare autosomal recessive multisystem disorder of pigmentary dilution of skin, silver gray hair, variable immunodeficiency, neurological impairment, and abnormal accumulation of melanosomes in melanocytes. GS type 3 is characterized by hypomelanosis with no immunological...

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Detalles Bibliográficos
Autores principales:	Shah, Bela J., Jagati, Ashish K., Katrodiya, Nilesh K., Patel, Sonal M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134165/ https://www.ncbi.nlm.nih.gov/pubmed/27990386 http://dx.doi.org/10.4103/2229-5178.193910

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