Griscelli Syndrome, 2
Definition
Biallelic pathogenic variants in the RAB27A gene render nonfunctional a Rab GTPase protein involved in the exocytosis of cytotoxic granules and melanosomes. The clinical picture includes partial albinism, cellular immune deficiency, and resulting episodes of hemophagocytic lymphohistiocytosis.
Gene/region examined
RAB27A - Exon 2, RAB27A - Exon 3, RAB27A - Exon 4, RAB27A - Exon 5, RAB27A - Exon 6
Method
Sequence analysis
Accepted sample types
EDTA blood, AF, CVS
Inheritance
Inherited, autosomal recessive.