Features of Hemophagocytic Lymphohistiocytosis in Infants With Severe Combined Immunodeficiency: Our Experience From Chandigarh, North India

BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is characterized by uncontrolled and excessive inflammation leading to high mortality. Aetiology of HLH can be primarily due to genetic causes or secondarily due to infections or rheumatological illness. However, rarely T-cell deficiencies like se...

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Detalles Bibliográficos
Autores principales: Vignesh, Pandiarajan, Anjani, Gummadi, Kumrah, Rajni, Singh, Ankita, Mondal, Sanjib, Nameirakpam, Johnson, Jindal, Ankur, Suri, Deepti, Sharma, Madhubala, Kaur, Gurjit, Sharma, Sathish, Gupta, Kirti, Sreedharanunni, Sreejesh, Rawat, Amit, Singh, Surjit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260510/
https://www.ncbi.nlm.nih.gov/pubmed/35812426
http://dx.doi.org/10.3389/fimmu.2022.867753

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260510/
https://www.ncbi.nlm.nih.gov/pubmed/35812426
http://dx.doi.org/10.3389/fimmu.2022.867753

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