Chromosome 22q11.21 and 11p15.4 microdeletions confirmed by high‐throughput sequencing analysis in one patient with asymmetric cry syndrome: Case report and review of the literature

Abstract

Abstract Healthcare providers treating newborns with asymmetric cry syndrome should consider 22q11.2 microdeletion within the differential diagnosis list and order appropriate genetic testing.

Keywords

• asymmetric cry syndrome
• high‐throughput sequencing
• microdeletion