Literature DB >> 18040716

A rare association of interrupted aortic arch type C and microdeletion 22q11.2.

Goran Cuturilo1, Danijela Drakulic, Milena Stevanovic, Ida Jovanovic, Milan Djukic, Slobodanka Miletic-Grkovic, Marina Atanaskovic-Markovic.   

Abstract

Microdeletion 22q11.2 is associated with a variety of findings, and the most common are cardiac defects. It is very frequently associated with interrupted aortic arch (IAA) type B and very rarely with type A and type C. Here we report the first case of IAA type C associated with 22q11.2 deletion in Serbia and, to the best of our knowledge, the fourth case described worldwide so far. By this report we would like to point out that all patients with IAA type C who have additional features specific for 22q11.2 microdeletion syndrome should be screened for the presence of this deletion.

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Year:  2007        PMID: 18040716     DOI: 10.1007/s00431-007-0632-7

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  13 in total

1.  A rare form of interrupted aortic arch.

Authors:  G Agnoletti; A Borghi; F Annecchino
Journal:  Ital Heart J       Date:  2001-03

2.  Guidelines for 22q11 deletion screening of patients with conotruncal defects.

Authors:  M C Digilio; B Marino; A Giannotti; R Mingarelli; B Dallapiccola
Journal:  J Am Coll Cardiol       Date:  1999-05       Impact factor: 24.094

3.  Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies.

Authors:  M C Digilio; A Angioni; M De Santis; A Lombardo; A Giannotti; B Dallapiccola; B Marino
Journal:  Clin Genet       Date:  2003-04       Impact factor: 4.438

4.  Frequency of inherited deletions of 22q11.

Authors:  P W Thompson; S J Davies
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

5.  Frequency of 22q11 deletions in patients with conotruncal defects.

Authors:  E Goldmuntz; B J Clark; L E Mitchell; A F Jawad; B F Cuneo; L Reed; D McDonald-McGinn; P Chien; J Feuer; E H Zackai; B S Emanuel; D A Driscoll
Journal:  J Am Coll Cardiol       Date:  1998-08       Impact factor: 24.094

Review 6.  Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2: report of five families with a review of the literature.

Authors:  J Leana-Cox; S Pangkanon; K R Eanet; M S Curtin; E A Wulfsberg
Journal:  Am J Med Genet       Date:  1996-11-11

7.  Deletion 22q11 in patients with interrupted aortic arch.

Authors:  B Marino; M C Digilio; M Persiani; R Di Donato; A Toscano; A Giannotti; B Dallapiccola
Journal:  Am J Cardiol       Date:  1999-08-01       Impact factor: 2.778

8.  Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch.

Authors:  A Rauch; M Hofbeck; G Leipold; J Klinge; U Trautmann; M Kirsch; H Singer; R A Pfeiffer
Journal:  Am J Med Genet       Date:  1998-07-24

9.  Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!

Authors:  D M McDonald-McGinn; M K Tonnesen; A Laufer-Cahana; B Finucane; D A Driscoll; B S Emanuel; E H Zackai
Journal:  Genet Med       Date:  2001 Jan-Feb       Impact factor: 8.822

10.  Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Authors:  A K Ryan; J A Goodship; D I Wilson; N Philip; A Levy; H Seidel; S Schuffenhauer; H Oechsler; B Belohradsky; M Prieur; A Aurias; F L Raymond; J Clayton-Smith; E Hatchwell; C McKeown; F A Beemer; B Dallapiccola; G Novelli; J A Hurst; J Ignatius; A J Green; R M Winter; L Brueton; K Brøndum-Nielsen; P J Scambler
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

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  1 in total

1.  Investigation of copy number variation in children with conotruncal heart defects.

Authors:  Carla Marques Rondon Campos; Evelin Aline Zanardo; Roberta Lelis Dutra; Leslie Domenici Kulikowski; Chong Ae Kim
Journal:  Arq Bras Cardiol       Date:  2014-11-11       Impact factor: 2.000

  1 in total

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