Griscelli Syndrome With Hemophagocytic Lymphohistiocytosis: A Rare Case Report

Griscelli syndrome type 2 (GS2) is a rare, autosomal recessive condition caused by a mutation of the RAB27A gene that causes primary immunodeficiency and pigmentary dilution of skin and hair. It is a rare occurrence, with only 160 cases reported all over the world. It commonly progresses to hemophag...

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Detalles Bibliográficos
Autores principales: Perugu, Ratna Krishna Tanmayi, Karra, Nanditha, Shaik, Saniya s, Venigalla, Womesh Chandra, G, Preeti, Maram, Manasvi Reddy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Dermatology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544088/
https://www.ncbi.nlm.nih.gov/pubmed/37791210
http://dx.doi.org/10.7759/cureus.44445

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544088/
https://www.ncbi.nlm.nih.gov/pubmed/37791210
http://dx.doi.org/10.7759/cureus.44445

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