22q11.2 deletion syndrome

22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency.

Myocarditis

Inflammation of the myocardium.


Total: 1

                       


(per page)
PMID (PMCID)
30397574
(6213892)
 OTHER
Clozapine-induced myocarditis in an adolescent male with DiGeorge Syndrome.
Ruhe AM, Qureshi I, Procaccini D.
Ment Health Clin. 2018;8(6):313-316.
Clozapine-induced myocarditis in an adolescent male with DiGeorge Syndrome.