Open AccessChromosome 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
Author(s) -
Pang Yonghong,
Yu Yang,
Deng Xiaoyi,
Liu Qian,
Yan Junmei,
Gao Xiangyu
Publication year - 2021
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.4072
Subject(s) - medicine , chromosome , deletion syndrome , genetic testing , microdeletion syndrome , genetics , gene , biology , phenotype
Abstract Healthcare providers treating newborns with asymmetric cry syndrome should consider 22q11.2 microdeletion within the differential diagnosis list and order appropriate genetic testing.