| Literature DB >> 32487530 |
Alberto Olivella1, Hernan Manotas2, César Payán-Gómez3, Juan Gabriel Piñeros4.
Abstract
Ebstein anomaly is a congenital heart defect with a low prevalence and high mortality in the early stages of life. In medical literature, there is no reported association between Ebstein anomaly and cri du chat syndrome. Here, we report the case of a full-term newborn with a low weight for his age and who had a prenatal diagnosis of Ebstein anomaly and a postnatal diagnosis of cri du chat syndrome and 20q duplication detected on array CGH. The patient required medical treatment with inotropic support, high-frequency ventilation and nitric oxide, with an adequate response. Surgical intervention was not needed. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: congenital disorders; genetic screening / counselling; genetics; neonatal intensive care
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Year: 2020 PMID: 32487530 PMCID: PMC7265000 DOI: 10.1136/bcr-2019-233766
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X