DISSEMINATED BCG INFECTION RESEMBLING LANGERHANS CELL HISTIOCYTOSIS IN AN INFANT WITH SEVERE COMBINED IMMUNODEFICIENCY: A Case Report-Reference-Cited by-同舟云学术

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DISSEMINATED BCG INFECTION RESEMBLING LANGERHANS CELL HISTIOCYTOSIS IN AN INFANT WITH SEVERE COMBINED IMMUNODEFICIENCY: A Case Report

Published:2004-01 Issue:6 Volume:21 Page:561-570
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Culic Srdjana,Kuzmic Ivana,Culic Vida,Martinic Roko,Kuljis Dubravka,Pranic-Kragic Ankica,Karaman Ksenija,Jankovic Stipan

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1080/08880010490477257

Reference16 articles.

1. Primary Immunodeficiency Diseases Due to Defects in Lymphocytes

2. Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infants

3. Diagnostic Criteria for Primary Immunodeficiencies

4. Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell–depleted bone marrow transplantationA retrospective European survey from the European Group for Bone Marrow Transplantation and the European Society for Immunodeficiency

5. Gene therapy of severe combined immunodeficiencies

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1. X-linked severe combined immunodeficiency complicated by disseminated bacillus Calmette-Guérin disease caused by a novel pathogenic mutation in exon 3 of the IL2RG gene: a case report and literature review;Frontiers in Immunology;2024-08-08

2. Assistance of next-generation sequencing for diagnosis of disseminated Bacillus Calmette-Guerin disease with X-SCID in an infant: a case report and literature review;Frontiers in Cellular and Infection Microbiology;2024-02-12

3. Metagenomic sequencing expedites diagnosis of disseminated BCG in an infant with BRAFV600E mutation;The Journal of Infection in Developing Countries;2024-01-31

4. Multiple Lytic Bone Lesions Mimicking Langerhans Cell Histiocytosis: A Case of Infantile Mendelian Susceptibility to Mycobacterial Disease due to STAT1 Deficiency;Open Forum Infectious Diseases;2022-10-11

5. Severe combined immunodeficiency (SCID): a case series from a paediatric hospital in Kenya;Pan African Medical Journal;2021

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