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The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India

Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of immune dysregulation characterized by hyperactivation of the immune system, excessive cytokine secretion and severe systemic inflammation. HLH is classified as familial (FHL) when associated with mutations in PRF1, UNC13D, STX11, and STXBP2 g...

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Detalles Bibliográficos
Autores principales: Shabrish, Snehal, Kelkar, Madhura, Yadav, Reetika Malik, Bargir, Umair Ahmed, Gupta, Maya, Dalvi, Aparna, Aluri, Jahnavi, Kulkarni, Manasi, Shinde, Shweta, Sawant-Desai, Sneha, Kambli, Priyanka, Hule, Gouri, Setia, Priyanka, Jodhawat, Neha, Gaikwad, Pallavi, Dhawale, Amruta, Nambiar, Nayana, Gowri, Vijaya, Pandrowala, Ambreen, Taur, Prasad, Raj, Revathi, Uppuluri, Ramya, Sharma, Ratna, Kini, Pranoti, Sivasankaran, Meena, Munirathnam, Deenadayalan, Vedam, Ramprasad, Vignesh, Pandiarajan, Banday, Aaqib, Rawat, Amit, Aggarwal, Amita, Poddar, Ujjal, Girish, Meenakshi, Chaudhary, Abhijit, Sampagar, Abhilasha, Jayaraman, Dharani, Chaudhary, Narendra, Shah, Nitin, Jijina, Farah, Chandrakla, S., Kanakia, Swati, Arora, Brijesh, Sen, Santanu, Lokeshwar, Madhukar, Desai, Mukesh, Madkaikar, Manisha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973116/
https://www.ncbi.nlm.nih.gov/pubmed/33746956
http://dx.doi.org/10.3389/fimmu.2021.612583

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