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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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| Publicado en: | Indian Dermatol Online J |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5134165/ https://ncbi.nlm.nih.gov/pubmed/27990386 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2229-5178.193910 |
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