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An Unusual Association: Total Anomalous Pulmonary Venous Return and Aortic Arch Obstruction in Patients with Cat Eye Syndrome.
Williams, Jason L; McDonald, Marie T; Seifert, Bryce A; Deak, Kristen L; Rehder, Catherine W; Campbell, Michael J.
Afiliação
  • Williams JL; Division of Pediatric Cardiology, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, United States.
  • McDonald MT; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, United States.
  • Seifert BA; Department of Pathology, Duke University Medical Center, Durham, North Carolina, United States.
  • Deak KL; Department of Pathology, Duke University Medical Center, Durham, North Carolina, United States.
  • Rehder CW; Department of Pathology, Duke University Medical Center, Durham, North Carolina, United States.
  • Campbell MJ; Division of Pediatric Cardiology, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, United States.
J Pediatr Genet ; 10(1): 35-38, 2021 Mar.
Article em En | MEDLINE | ID: mdl-33552636
Cat eye syndrome (CES) is a rare genetic defect, characterized by iris colobomas, preauricular skin tags, and anal malformations. Affecting 1 in 150,000 people, this defect is caused by duplication or triplication of the proximal long (q) arm of chromosome 22. Congenital heart disease is associated with CES. One of the most common heart defects in patients with CES is total anomalous pulmonary venous return (TAPVR). In this article, we reported patients with a rare association of concomitant TAPVR and aortic arch obstruction: one with interrupted aortic arch and the other with coarctation of the aorta with an aberrant right subclavian artery.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: J Pediatr Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: J Pediatr Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos