Gerbode ventricular septal defect –a rare cardiac anomaly associated with genetic variants in indian population- a case series

Yashvanthi Borkar, Krishnananda Nayak, Ranjan K. Shetty, Gopalakrishna Bhat, Rajasekhar Moka

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Gerbode defects are rare Ventricular Septal Defects (VSD) constituting approximately one percent cases of congenital heart diseases. The genetic predispositions towards the Gerbode Defect (GD) have remained an unexplored area of study till date. We investigated the genotype-phenotype correlation in patients with Gerbode VSD. Molecular genetic study on Sanger sequencing and subsequent data analysis showed that the contributing sequence variations in the NKX2-5, GATA4 and TBX5 gene lies in one of the highly conserved regions and this region is responsible for encoding a functional protein. The resulting genotype variation may be responsible for causing the diseased phenotype known as GD.

Original languageEnglish
Pages (from-to)GR01-GR04
JournalJournal of Clinical and Diagnostic Research
Volume11
Issue number3
DOIs
Publication statusPublished - 01-03-2017

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Ventricular Heart Septal Defects
Defects
Genetic Association Studies
Genetic Predisposition to Disease
Population
Molecular Biology
Heart Diseases
Genotype
Phenotype
Genes
Proteins

All Science Journal Classification (ASJC) codes

  • Clinical Biochemistry

Cite this

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Gerbode ventricular septal defect –a rare cardiac anomaly associated with genetic variants in indian population- a case series. / Borkar, Yashvanthi; Nayak, Krishnananda; Shetty, Ranjan K.; Bhat, Gopalakrishna; Moka, Rajasekhar.

In: Journal of Clinical and Diagnostic Research, Vol. 11, No. 3, 01.03.2017, p. GR01-GR04.

Research output: Contribution to journalArticle

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