Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review-Reference-Cited by-同舟云学术

Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review

Published:2020-08-24 Issue:1 Volume:32 Page:186-197
ISSN:0905-6157
Container-title:Pediatric Allergy and Immunology
language:en
Short-container-title:Pediatr Allergy Immunol

Author:

Amirifar Parisa¹²^ORCID,Ranjouri Mohammad Reza²,Abolhassani Hassan³⁴,Moeini Shad Tannaz²,Almasi‐Hashiani Amir⁵,Azizi Gholamreza²⁶^ORCID,Moamer Soraya⁷,Aghamohammadi Asghar²^ORCID,Yazdani Reza²^ORCID

Affiliation:

1. Department of Medical Genetics School of MedicineTehran University of medical sciences Tehran Iran

2. Research Center for ImmunodeficienciesPediatrics Center of ExcellenceChildren's Medical Center, Tehran University of Medical Sciences Tehran Iran

3. Research Center for Primary ImmunodeficienciesIran University of medical sciences Tehran Iran

4. Division of Clinical Immunology Department of Laboratory Medicine Karolinska Institute at Karolinska University Hospital Huddinge Stockholm Sweden

5. Department of Epidemiology Arak University of Medical Sciences Arak Iran

6. Non‐Communicable Diseases Research CenterAlborz University of Medical Sciences Karaj Iran

7. School of Public Health Student Research Committee Hamadan University of Medical Sciences Hamadan Iran

Publisher

Wiley

Subject

Immunology,Immunology and Allergy,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pai.13323

Reference56 articles.

1. The 253-kb inversion and deep intronic mutations inUNC13Dare present in North American patients with familial hemophagocytic lymphohistiocytosis 3

2. The Role of Infections in Primary Hemophagocytic Lymphohistiocytosis: A Case Series and Review of the Literature

3. Genetic variant spectrum in 265 Chinese patients with hemophagocytic lymphohistiocytosis: Molecular analyses of PRF1 , UNC13D , STX11 , STXBP2 , SH2D1A , and XIAP

4. Diagnostic challenges in a child with familial hemophagocytic lymphohistiocytosis type 3 (FHLH3) presenting with fulminant neurological disease

5. Familial Hemophagocytic Lymphohistiocytosis due to Mutation of UNC13D Gene

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