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.

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Bibliographic Details
Published in:Clinical case reports 2021, Vol.9 (5), p.e04072-e04072
Main Authors: Pang, Yonghong, Yu, Yang, Deng, Xiaoyi, Liu, Qian, Yan, Junmei, Gao, Xiangyu
Format: Report
Language:English
Online Access:Get full text
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Description
Summary:Healthcare providers treating newborns with asymmetric cry syndrome should consider 22q11.2 microdeletion within the differential diagnosis list and order appropriate genetic testing.
ISSN:2050-0904
2050-0904
DOI:10.1002/ccr3.4072