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.

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