Literature DB >> 15283354

Tetralogy of Fallot with absent pulmonary valve syndrome.

Paul M Kirshbom1, Brian E Kogon.   

Abstract

Tetralogy of Fallot with absent pulmonary valve syndrome is a rare variant of tetralogy of Fallot marked by severe pulmonary insufficiency in utero and significant, sometimes massive, dilation of the pulmonary arteries. This syndrome can be associated with airway abnormalities that can cause respiratory compromise. Patients who present with respiratory symptoms early in life continue to present a major clinical challenge associated with relatively high mortality rates, typically in the 20% to 30% range. A variety of surgical techniques have been developed to address absent pulmonary valve syndrome that may improve long-term outcomes.

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Year:  2004        PMID: 15283354     DOI: 10.1053/j.pcsu.2004.02.010

Source DB:  PubMed          Journal:  Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu        ISSN: 1092-9126


  6 in total

1.  Newborn with tetralogy of Fallot and absent pulmonary valve.

Authors:  Paul Chen; Maria Ladino-Torres
Journal:  Pediatr Radiol       Date:  2010-11-02

2.  Prenatal diagnosis of a patient with tetralogy of Fallot and an absent pulmonary valve.

Authors:  Cemşit Karakurt; Gülendam Koçak; Ozlem Elkiran
Journal:  Pediatr Cardiol       Date:  2010-12-25       Impact factor: 1.655

3.  Surgical outcome after complete repair of tetralogy of Fallot with absent pulmonary valve: comparison between bovine jugular vein-valved conduit and monocusp-valve patch.

Authors:  En-Shi Wang; Xue-Song Fan; Li Xiang; Shou-Jun Li; Hao Zhang
Journal:  World J Pediatr       Date:  2018-07-30       Impact factor: 2.764

4.  Echocardiography in the diagnosis of patients with absent pulmonary valve syndrome: a review study of 12 years.

Authors:  Weichun Wu; Kunjing Pang; Qiongwen Lin; Ani Zhang; Wugang Wang; Minghui Zhang; Jianrong Li; Hao Wang
Journal:  Int J Cardiovasc Imaging       Date:  2015-07-02       Impact factor: 2.357

5.  Surgical outcomes of absent pulmonary valve syndrome: An institutional experience.

Authors:  Ashvin Krishna Nair; Maruti Haranal; Ibrahim Mukhtar Elkhatim; Jeswant Dillon; Chee Chin Hew; Sivakumar Sivalingam
Journal:  Ann Pediatr Cardiol       Date:  2020-06-23

6.  Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease.

Authors:  Dimuthu Alankarage; Justin O Szot; Nick Pachter; Anne Slavotinek; Licia Selleri; Joseph T Shieh; David Winlaw; Eleni Giannoulatou; Gavin Chapman; Sally L Dunwoodie
Journal:  Hum Mol Genet       Date:  2020-05-08       Impact factor: 6.150

  6 in total

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