GRISCELLI SYNDROME TYPE 2 –CLINICAL APPROACH AND CASE REPORT

GRISCELLI SYNDROME TYPE 2 –CLINICAL APPROACH AND CASE REPORT

Objective: Griscelli syndrome type 2 is rare authosomal ressesive disorder caused by a defect in the RAB27A gene, which affects a melanosome-anchoring complex in melanocytes, affecting release of cytolytic granules from T and NK cells. Children with GS type 2 develop an uncontrolled T-lymphocyte and...

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Bibliographic Details
Main Authors: Konul Baghirova, Gular Mammadova, Avesta Allahverdiyeva, Narmin Eyvazova, Narmin Verdiyeva, Agarza Agayev, Samira Hasanova, Valeh Huseynov
Format: Article
Language:English
Published: Elsevier 2022-10-01
Series:Hematology, Transfusion and Cell Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S2531137922013876

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http://www.sciencedirect.com/science/article/pii/S2531137922013876

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