Chromosome 22q11 Microdeletions in Tetralogy of Fallot

Overview

Journal Arch Dis Child

Specialty Pediatrics

Date 1996 Jan 1

PMID 8660052

Citations 11

Authors

A H Trainer

N Morrison

A Dunlop

N Wilson

J Tolmie

Affiliations

Soon will be listed here.

Abstract

Chromosome 22q11 fluorescence in situ hybridisation (FISH) studies were performed on 33 consecutive individuals attending a paediatric cardiology clinic with tetralogy of Fallot. Seven children had 22q11 microdeletions but only four had other clinical features associated with the newly recognised chromosome 22 deletion syndrome (CATCH 22). Chromosome 22q11 FISH studies should therefore be performed on all patients with tetralogy of Fallot.

Citing Articles

Comparison of Postoperative, In-Hospital Outcomes After Complete Repair of Tetralogy of Fallot Between 22q11.2 Deletion Syndrome and Trisomy 21.

Nissen T, Zaniletti I, Collins 2nd R, Greiten L, Prodhan P, Seib P Pediatr Cardiol. 2021; 43(2):290-300.

PMID: 34331082 DOI: 10.1007/s00246-021-02683-1.

22q11.2 Deletion Status and Perioperative Outcomes for Tetralogy of Fallot with Pulmonary Atresia and Multiple Aortopulmonary Collateral Vessels.

Mercer-Rosa L, Elci O, Pinto N, Tanel R, Goldmuntz E Pediatr Cardiol. 2018; 39(5):906-910.

PMID: 29520463 PMC: 5959773. DOI: 10.1007/s00246-018-1840-9.

Dysphagia in an Adult Tetralogy of Fallot with Double aortic arch.

Pankaj B, Munesh T, Bhan A Images Paediatr Cardiol. 2015; 15(3):6-13.

PMID: 26236362 PMC: 4521333.

Ductal stent implantation in tetralogy of fallot with aortic arch abnormality.

Tola H, Ergul Y, Saygi M, Ozyilmaz I, Guzeltas A, Odemis E Tex Heart Inst J. 2015; 42(3):281-4.

PMID: 26175649 PMC: 4473630. DOI: 10.14503/THIJ-13-3373.

22q11.2 Deletion syndrome is associated with perioperative outcome in tetralogy of Fallot.

Mercer-Rosa L, Pinto N, Yang W, Tanel R, Goldmuntz E J Thorac Cardiovasc Surg. 2013; 146(4):868-73.

PMID: 23312975 PMC: 3706509. DOI: 10.1016/j.jtcvs.2012.12.028.

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