Literature DB >> 9316541

Truncus arteriosus communis associated with chromosome 22q11 deletion.

K Momma1, M Ando, R Matsuoka.   

Abstract

OBJECTIVES: The purpose of this study was to clarify characteristics of truncus arteriosus communis associated with chromosome 22q11 deletion (del 22q11).
BACKGROUND: DiGeorge syndrome and conotruncal anomaly face syndrome are associated with del 22q11 (hemizygosity). In 30% of cases, truncus arteriosus communis is associated with the deletion.
METHODS: Fifteen consecutive patients with truncus arteriosus communis were checked for 22q11 with fluorescent in situ hybridization using an N25 probe (Oncor). Cardiovascular anomalies were studied with cardiac catheterization, cineangiography and echocardiography.
RESULTS: Five patients had del 22q11. Two had a rare type of truncus arteriosus: type A3 of Van Praagh and Van Praagh with major aortopulmonary collateral arteries and pulmonary ostial stenosis. The other three had type A1 truncus arteriosus and pulmonary artery stenosis. One of them had major aortopulmonary collateral arteries. Ten patients with truncus arteriosus had no del 22q11. The types of truncus arteriosus in these 10 patients were type A1 in 7, type A2 in 2 and type A3 with closed ductus in 1. None of nine patients with type 1 or type 2 truncus arteriosus had pulmonary stenosis.
CONCLUSIONS: In truncus arteriosus communis, the rare type A3 with major aortopulmonary collateral arteries and pulmonary ostial stenosis and type A1 with pulmonary artery stenosis are associated with del 22q11.

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Mesh:

Year:  1997        PMID: 9316541     DOI: 10.1016/s0735-1097(97)00240-4

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  15 in total

1.  Truncus arteriosus communis in a midtrimester fetus: comparison of prenatal ultrasound and MRI with postmortem MRI and autopsy.

Authors:  Matthias R Mühler; Anett Rake; Michael Schwabe; Rabih Chaoui; Kay-Sven Heling; Christiane Planke; Alexander Lembcke; Thomas Fischer; Dietmar Kivelitz
Journal:  Eur Radiol       Date:  2004-10-06       Impact factor: 5.315

2.  Chromosome 22q11 deletions in patients with conotruncal heart defects.

Authors:  A Khositseth; C Tocharoentanaphol; P Khowsathit; N Ruangdaraganon
Journal:  Pediatr Cardiol       Date:  2005 Sep-Oct       Impact factor: 1.655

3.  An unusual and rare form of truncus arteriosus in an asymptomatic woman.

Authors:  Maryam Nabati
Journal:  Ultrasound       Date:  2017-06-01

4.  GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling.

Authors:  Kazuki Kodo; Tsutomu Nishizawa; Michiko Furutani; Shoichi Arai; Eiji Yamamura; Kunitaka Joo; Takao Takahashi; Rumiko Matsuoka; Hiroyuki Yamagishi
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-04       Impact factor: 11.205

Review 5.  Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

Authors:  Marta Unolt; Paolo Versacci; Silvia Anaclerio; Caterina Lambiase; Giulio Calcagni; Matteo Trezzi; Adriano Carotti; Terrence Blaine Crowley; Elaine H Zackai; Elizabeth Goldmuntz; James William Gaynor; Maria Cristina Digilio; Donna M McDonald-McGinn; Bruno Marino
Journal:  Am J Med Genet A       Date:  2018-04-16       Impact factor: 2.802

6.  Prenatal diagnosis of truncus arteriosus using multiplanar display in 4D ultrasonography.

Authors:  Francesca Gotsch; Roberto Romero; Jimmy Espinoza; Juan Pedro Kusanovic; Offer Erez; Sonia Hassan; Lami Yeo
Journal:  J Matern Fetal Neonatal Med       Date:  2010-04

7.  Chromosome 22q11 deletion in patients with truncus arteriosus.

Authors:  D B McElhinney; D A Driscoll; B S Emanuel; E Goldmuntz
Journal:  Pediatr Cardiol       Date:  2003-09-04       Impact factor: 1.655

8.  Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.

Authors:  Lidia Ziolkowska; Wanda Kawalec; Anna Turska-Kmiec; Malgorzata Krajewska-Walasek; Grazyna Brzezinska-Rajszys; Jadwiga Daszkowska; Bogdan Maruszewski; Piotr Burczynski
Journal:  Eur J Pediatr       Date:  2008-01-03       Impact factor: 3.183

9.  Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes?

Authors:  Ralf Rauch; Anita Rauch; Andreas Koch; Stefan Zink; Renate Kaulitz; Monika Girisch; Helmut Singer; Michael Hofbeck
Journal:  Eur J Pediatr       Date:  2004-08-06       Impact factor: 3.183

10.  Chromosomal abnormalities among children born with conotruncal cardiac defects.

Authors:  Edward J Lammer; Jacqueline S Chak; David M Iovannisci; Kathleen Schultz; Kazutoyo Osoegawa; Wei Yang; Suzan L Carmichael; Gary M Shaw
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-01
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