Ojaimi S

ORCID: 0000-0003-2129-1866 · 1 paper in corpus
2024
Internal medicine journal ·doi:10.1111/imj.16534

BackgroundChromosome 22q11.2 deletion syndrome (22q11DS) is the most common microdeletion syndrome, typically presenting in neonates with congenital cardiac anomalies, hypocalcaemia and thymic hypoplasia. Some patients are diagnosed later i…