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

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

Source: Clinical Case Reports - March 28, 2021 Category: General Medicine Authors: Yonghong Pang, Yang Yu, Xiaoyi Deng, Qian Liu, Junmei Yan, Xiangyu Gao Tags: CASE REPORT Source Type: research