A novel mutated sequence in the T-box transcription factor-5 (TBX-5) gene (c.241A>T) in Holt–Oram syndrome

• Published in: Journal of the Turkish German Gynecological Association Vol. 17; no. 1; pp. 55 - 57
• Main Authors: Ersoy, Ali Ozgur, Topcu, Vehap, Kale, Ibrahim, Ersoy, Ebru, Ozler, Sibel, Danisman, Nuri
• Format: Journal Article
• Language: English
• Published: Istanbul Galenos Publishing House 01-03-2016; AVES
• Subjects: Case Report
• ISSN: 1309-0399; 1309-0380
• DOI: 10.5152/jtgga.2015.15233

We report a case of a 31-year-old pregnant woman who was admitted to our perinatology outpatient clinic because of a fetal ventricular septal defect and limb reduction in the upper extremities of fetus revealed by ultrasonographic investigation diagnosed in the 16
th
week of gestation. First child of the family was diagnosed with Holt–Oram syndrome who had atrial septal defect and upper limb anomalies, whereas the father was documented to have arrhythmia and shortening of upper limbs. The pregnancy was terminated in the 16
th
week of gestation with the consent of the family. We performed mutation analysis in
T-box transcription factor-5 (TBX5)
gene coding exons, including exon/intron boundaries from peripheral blood or skin fibroblasts. The sequence analysis revealed c.241 adenine (A)>thymine (T) [p. arginine (Arg) 81 Tryptophan (Trp)] alteration in exon-3 of the
TBX5
gene in affected family members and fetus. This is a novel mutation causing Holt–Oram syndrome.