Article

Hemophagocytic Lymphohistiocytosis in Children with Griscelli Syndrome Type 2 : Genetic, Laboratory findings and Treatment

2023-03-28

Abstract excerpt

Griscelli syndrome is a rare autosomal recessive inherited syndrome that causes immunodeficiency. Hemophagocytic lymphohistiocytosis (HLH), which is characterized by high mortality, may develop due to Griscelli syndrome type 2 (GS2). We aimed to share our experience in diagnosis and treatment methods of patients who developed HLH secondary to GS2. GS2 patients

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: bdb29135-c6b9-5821-813d-3121c5ce1ab1
DOI: 10.22541/au.167999769.92862924/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Hemophagocytic Lymphohistiocytosis in Children with Griscelli Syndrome Type 2 : Genetic, Laboratory findings and TreatmentDOI 10.22541/au.167999769.92862924/v1Read

Pulmonary lymphomatoid granulomatosis in Griscelli syndrome type 2.Semantic proximity Read

Griscelli Syndrome Type 2: Comprehensive Analysis of 149 New and Previously Described Patients with RAB27A Deficiency.Semantic proximity Read

Primary Hemophagocytic Lymphohistiocytosis: A Severe Immune Dysregulatory Disease with Various Genotypic Features and Outcomes: A Cross-Sectional Study from a Tertiary Pediatric CenterSemantic proximity Read

Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult-Onset in a 46-Year-Old Male.Semantic proximity Read

[Association between genotype and clinical phenotype in children with primary hemophagocytic lymphohistiocytosis].Semantic proximity Read

Molecular analysis and clinical findings of Griscelli syndrome patients.Semantic proximity Read

Macrophage activation syndrome associated with griscelli syndrome type 2: case report and review of literature.Semantic proximity Read

Hemophagocytic Lymphohistiocytosis: Lessons Learned from the Dark Side.Semantic proximity Read

Hemophagocytic Lymphohistiocytosis in Adolescents and Young Adults: Genetic Predisposition and Secondary Disease.Semantic proximity Read

Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient.Semantic proximity Read

Current Updates on Classification, Diagnosis and Treatment of Hemophagocytic Lymphohistiocytosis (HLH)Semantic proximity Read

A novel RAB27A mutation in a patient with Griscelli syndrome type 2.Semantic proximity Read