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Case Report: Identification of microduplication in the chromosomal 2p16.1p15 region in an infant suffering from pulmonary arterial hypertension
This study reports the first case of a patient with chromosomal 2p16.1p15 microduplication syndrome complicated by pulmonary arterial hypertension (PAH). A female infant was admitted to the hospital suffering from dyskinesia and developmental delay, and conventional echocardiography revealed an atri...
Autores principales: | Wang, Xun, Zhang, Zeying, Zuo, Wanyun, Wang, Dan, Yang, Fan, Liu, Qiming, Xiao, Yunbin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626460/ https://www.ncbi.nlm.nih.gov/pubmed/37937284 http://dx.doi.org/10.3389/fcvm.2023.1219480 |
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