Familial hemophagocytic lymphohistiocytosis type 3 presenting as neonatal cholestasis and splenomegaly-Reference-Cited by-同舟云学术

Familial hemophagocytic lymphohistiocytosis type 3 presenting as neonatal cholestasis and splenomegaly

Published:2022-04 Issue:4 Volume:33 Page:
ISSN:0905-6157
Container-title:Pediatric Allergy and Immunology
language:en
Short-container-title:Pediatric Allergy Immunology

Author:

Bogaert Delfien¹²^ORCID,De Bruyne Ruth³^ORCID,Vanlander Arnaud V.⁴^ORCID,Garabedian Lara⁵,Louis Yves⁶,Haerynck Filomeen²⁷^ORCID,Bordon Victoria¹^ORCID,De Moerloose Barbara¹^ORCID

Affiliation:

1. Division of Pediatric Hemato‐Oncology and Stem Cell Transplantation Department of Pediatrics Ghent University Hospital Ghent Belgium

2. Primary Immunodeficiency Research Lab Center for Primary Immunodeficiency Ghent Jeffrey Modell Diagnosis and Research Center Ghent University Hospital Ghent Belgium

3. Division of Gastroenterology and Hepatology Department of Pediatrics Ghent University Hospital Ghent Belgium

4. Division of Pediatric Neurology and Metabolism Department of Pediatrics Ghent University Hospital Ghent Belgium

5. Neonatal Intensive Care Unit Ghent University Hospital Ghent Belgium

6. Department of Pediatrics General Hospital Glorieux Ronse Belgium

7. Division of Pediatric Pulmonology Immunology and Infectious Diseases, Department of Pediatrics Ghent University Hospital Ghent Belgium

Publisher

Wiley

Subject

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pai.13774

Reference11 articles.

1. Pediatric hemophagocytic lymphohistiocytosis

2. Wolman disease associated with hemophagocytic lymphohistiocytosis: attempts for an explanation

3. Recommendations for the Use of Etoposide-Based Therapy and Bone Marrow Transplantation for the Treatment of HLH: Consensus Statements by the HLH Steering Committee of the Histiocyte Society

4. A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes

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

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