Literature DB >> 11509848

Pulmonary atresia with hypoplastic right ventricle. A clinical embryological study.

R Fröber1, T Kohoutek, C Kähler, V Beensen, R Hauschild, E Schulze, W Linss.   

Abstract

An unusual case of pulmonary atresia with an aberrant karyotype of 46,XX,t(6;8)(p21.2;q11.2) is reported. Fetal ultrasonic examination at the 20th week of gestation revealed a hypoplastic right ventricle and an intact interventricular septum. Authors summarize their postnatal findings in fetal heart and the large adjacent vessels with special reference to the pathogenesis of this rare congenital heart defect. The observation delineates right-ventricular outflow tract obstruction associated with an abnormal pulmonary blood supply. The anatomy of the systemic pulmonary collaterals was studied and correlated with multifocal disorders in the system of the pharyngeal arch arteries in the early embryonic development. Copyright 2001 S. Karger AG, Basel

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Year:  2001        PMID: 11509848     DOI: 10.1159/000053927

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  1 in total

1.  Pulmonary atresia with intact ventricular septum and major aortopulmonary collaterals: association with deletion 22q11.2.

Authors:  C Li; A E Chudley; R Soni; A Divekar
Journal:  Pediatr Cardiol       Date:  2003-07-29       Impact factor: 1.655

  1 in total

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