Journal of Blood Disorders & Transfusion

Journal of Blood Disorders & Transfusion
Open Access

ISSN: 2155-9864

+44 7460731551

Abstract

Genetic Hemophagocytic Lymphohistiocytosis with Syntaxin Gene Mutation

Rabia Ahmad*, Asma Akhter, Ahmad Saleem and Ambereen Anwar

We report a case of 5-year-old male who presented with off and on fever and bleeding. On examination he had oral ulcers and hepatosplenomegaly. One of his brothers who died at the age of one year, had similar complaints. Bone marrow examination of the child revealed hemophagocytosis. He was subsequently diagnosed as having Hemophagocytic Lymphohistiocytosis and next generation sequencing identified a rare 173T>C;p.Leu58Pro mutation in STX11genes in homozygous state resulting in familial or genetic HLH.

Published Date: 2019-09-30; Received Date: 2019-08-12

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