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Pulmonary artery sling in a 22-month-old boy with 18q deletion syndrome: A rare but possible association.
Delogu, Angelica Bibiana; Mariani, Francesco; Graziani, Francesca; Onesimo, Roberta; Savino, Giancarlo; Leoni, Chiara; Zampino, Giuseppe.
Afiliação
  • Delogu AB; Unit of Pediatrics, Pediatric Cardiology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Mariani F; Università Cattolica del Sacro Cuore, Rome, Italy.
  • Graziani F; Unit of Pediatrics, Pediatric Cardiology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Onesimo R; Università Cattolica del Sacro Cuore, Rome, Italy.
  • Savino G; Department of Cardiovascular and Thoracic Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Leoni C; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Zampino G; Section of Radiology, Department of Radiological and Hematological Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Echocardiography ; 39(5): 741-744, 2022 05.
Article em En | MEDLINE | ID: mdl-35434845
ABSTRACT
The 18q deletion syndrome is a rare genetic condition characterized by a large variability in clinical phenotype and severity. Congenital heart diseases have been described by several previous reports, most commonly including pulmonary valve anomalies and septal defects. We describe a new case of a 22-month-old boy affected by 18q del syndrome found to have a symptomatic pulmonary artery sling. This study reports a new case of pulmonary artery sling associated with 18q del syndrome, providing an alert for pediatric cardiologists about less common cardiovascular anomalies, which can easily be missed, allowing for early diagnosis and appropriate care.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Cromossômicos / Malformações Vasculares / Cardiopatias Congênitas Tipo de estudo: Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Cromossômicos / Malformações Vasculares / Cardiopatias Congênitas Tipo de estudo: Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article