SOCS1 Haploinsufficiency Presenting As Incidental Refractory Thrombocytopenia in a Pediatric Patient with Inflammatory Symptoms and History of Sars Cov-2 Infection

BACKGROUND: Immune thrombocytopenia purpura (ITP) has a complex pathogenesis and may be a primary diagnosis or secondary to an underlying condition (1). Evaluation for underlying diagnoses in patients presenting with atypical features of classic ITP is key, as this can impact treatment decisions, th...

Descripción completa

Detalles Bibliográficos
Autores principales: Lapinski, Jillian, Ngo, Sandra Hoang, Lee, Pui Y, Walkovich, Kelly J., Hannibal, Mark, DeMeyer, Lauren, Mohan, Smriti, Michniacki, Thomas F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology. Published by Elsevier Inc. 2021
Materias:
311.Disorders of Platelet Number or Function: Clinical and Epidemiological
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701427/
http://dx.doi.org/10.1182/blood-2021-153035

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701427/
http://dx.doi.org/10.1182/blood-2021-153035

Ejemplares similares