Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome

OBJECTIVE: To analyze the spectrum of prenatally diagnosed congenital heart disease in a Korean population with 22q11.2 deletion syndrome, and to provide guidelines for screening 22q11.2 deletion prenatally. METHODS: This retrospective study evaluated 1,137 consecutive fetuses that had prenatal gene...

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Detalhes bibliográficos
Main Authors: Lee, Mi-Young, Won, Hye-Sung, Baek, Ju Won, Cho, Jae-Hyun, Shim, Jae-Yoon, Lee, Pil-Ryang, Kim, Ahm
Formato: Artigo
Idioma:Inglês
Publicado em: Korean Society of Obstetrics and Gynecology; Korean Society of Contraception and Reproductive Health; Korean Society of Gynecologic Endocrinology; Korean Society of Gynecologic Endoscopy and Minimal Invasive Surgery; Korean Society of Maternal Fetal Medicine; Korean Society of Ultrasound in Obstetrics and Gynecology; Korean Urogynecologic Society 2014
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3924741/
https://ncbi.nlm.nih.gov/pubmed/24596813
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5468/ogs.2014.57.1.11
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