SOCS1 Haploinsufficiency Presenting as Severe Enthesitis, Bone Marrow Hypocellularity, and Refractory Thrombocytopenia in a Pediatric Patient with Subsequent Response to JAK Inhibition-Reference-Cited by-同舟云学术

SOCS1 Haploinsufficiency Presenting as Severe Enthesitis, Bone Marrow Hypocellularity, and Refractory Thrombocytopenia in a Pediatric Patient with Subsequent Response to JAK Inhibition

Published:2022-08-17 Issue:8 Volume:42 Page:1766-1777
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

Michniacki Thomas F.^ORCID,Walkovich Kelly,DeMeyer Lauren,Saad Nadine,Hannibal Mark,Basiaga Matthew L.,Horst Kelly K.,Mohan Smriti,Chen Liang,Brodeur Kailey,Du Yan,Frame David,Ngo Sandra,Simoneau Jillian,Brown Noah,Lee Pui Y.

Funder

National Institute of Health / National Institute of Arthritis and Musculoskeletal and Skin Diseases

Charles H. Hood Foundation Child Health Research Award

Arthritis National Research Foundation All Arthritis Grant

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

https://link.springer.com/content/pdf/10.1007/s10875-022-01346-x.pdf

Reference35 articles.

1. Lee PY, et al. Immune dysregulation and multisystem inflammatory syndrome in children (MIS-C) in individuals with haploinsufficiency of SOCS1. J Allergy Clin Immunol. 2020;146(5):1194-1200.e1. https://doi.org/10.1016/j.jaci.2020.07.033.