Familial transposition of the great arteries caused by multiple mutations in laterality genes. Issue 9 (20th November 2009)

• Record Type: Journal Article
• Authors: De Luca, Alessandro; Sarkozy, Anna; Consoli, Federica; Ferese, Rosangela; Guida, Valentina; Dentici, Maria Lisa; Mingarelli, Rita; Bellacchio, Emanuele; Tuo, Giulia; Limongelli, Giuseppe; Digilio, Maria Cristina; Marino, Bruno; Dallapiccola, Bruno
• Is Part Of: Heart. Volume 96:Issue 9(2010)
• Page Start: 673
• Page End: 677
• Publication Date: 2009-11-20
• Subjects: Congenital heart disease -- genetics -- molecular genetics -- mutation -- transportation of the great arteries -- transposition of great vessels; Heart -- Diseases -- Treatment -- Periodicals; Cardiology -- Periodicals; 616.12
• DOI: 10.1136/hrt.2009.181685
• Languages: English
• ISSNs: 1355-6037

Abstract

Abstract : Background: The pathogenesis of transposition of the great arteries (TGA) is still largely unknown. In general, TGA is not associated with the more common genetic disorders nor with extracardiac anomalies, whereas it can be found in individuals with lateralisation defects, heterotaxy and asplenia syndrome (right isomerism). Objective: To analyse genes previously associated with heterotaxy in order to assess mutations in familial TGA unassociated with other features of laterality defects. Methods: Probands of seven families with isolated TGA and a family history of concordant or discordant congenital heart disease were screened for mutations in the ZIC3, ACVR2B, LEFTYA, CFC1, NODAL, FOXH1, GDF1, CRELD1, GATA4 and NKX2.5 genes. Results: Mutation analysis allowed the identification of three sequence variations in two out of seven TGA probands. A FOXH1 (Pro21Ser) missense variant was found in a proband who was also heterozogous for an amino acid substitution (Gly17Cys) in the ZIC3 gene. This ZIC3 variant was also found in another family member with a second sequence variation (Val150Ile) in the NKX2.5 gene homeodomain who was affected by multiple ventricular septal defects. A second proband was found to harbour a splice site variant (IVS2-1G→C) in the NODAL gene. Conclusions: The present study provides evidence that some cases of familial TGA are caused by mutations in laterality genes and therefore are part of the same disease spectrum of heterotaxy syndrome, and argues for an oligogenic or complex mode of inheritance in these pedigrees.