Evans syndrome in the background of 22q11.2 deletion syndrome

Pediatr Blood Cancer. 2024 Jul;71(7):e31049. doi: 10.1002/pbc.31049. Epub 2024 May 6.

Authors

Mohmmad M Alawajneh¹, Waseem Sameer¹, Mohamed Al Zobi¹, Eesha A Zaheer², Ravi Talati³, Harry Lesmana^{3

4}

Affiliations

¹ Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
² Cleveland Clinic Foundation, Department of Pediatrics, Pediatric Institute, Cleveland, Ohio, USA.
³ Cleveland Clinic Foundation, Department of Pediatric Hematology, Oncology, and BMT, Pediatric Institute, Cleveland, Ohio, USA.
⁴ Cleveland Clinic Foundation, Center for Personalized Genetic Healthcare, Medical Specialty Institute, Cleveland, Ohio, USA.

PMID: 38711190
DOI: 10.1002/pbc.31049

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Anemia, Hemolytic, Autoimmune* / genetics
Anemia, Hemolytic, Autoimmune* / pathology
Child
Chromosomes, Human, Pair 22 / genetics
DiGeorge Syndrome* / complications
DiGeorge Syndrome* / genetics
DiGeorge Syndrome* / pathology
Female
Humans
Male
Thrombocytopenia* / genetics
Thrombocytopenia* / pathology

Supplementary concepts

Evans Syndrome