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.

Detalles Bibliográficos
Autores principales: Pang, Yonghong, Yu, Yang, Deng, Xiaoyi, Liu, Qian, Yan, Junmei, Gao, Xiangyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142403/
https://www.ncbi.nlm.nih.gov/pubmed/34084494
http://dx.doi.org/10.1002/ccr3.4072
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author Pang, Yonghong
Yu, Yang
Deng, Xiaoyi
Liu, Qian
Yan, Junmei
Gao, Xiangyu
author_facet Pang, Yonghong
Yu, Yang
Deng, Xiaoyi
Liu, Qian
Yan, Junmei
Gao, Xiangyu
author_sort Pang, Yonghong
collection PubMed
description 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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spelling pubmed-81424032021-06-02 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 Pang, Yonghong Yu, Yang Deng, Xiaoyi Liu, Qian Yan, Junmei Gao, Xiangyu Clin Case Rep Case Reports Healthcare providers treating newborns with asymmetric cry syndrome should consider 22q11.2 microdeletion within the differential diagnosis list and order appropriate genetic testing. John Wiley and Sons Inc. 2021-03-28 /pmc/articles/PMC8142403/ /pubmed/34084494 http://dx.doi.org/10.1002/ccr3.4072 Text en © 2021 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Pang, Yonghong
Yu, Yang
Deng, Xiaoyi
Liu, Qian
Yan, Junmei
Gao, Xiangyu
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
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142403/
https://www.ncbi.nlm.nih.gov/pubmed/34084494
http://dx.doi.org/10.1002/ccr3.4072
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