TGF-beta-activated kinase 1/MAP3K7-binding protein 2 (TAB 2 gene) deletion cause cardiac, especially valvular abnormalities and extracardiac abnormalities (distinctive facial features hypotonia, growth abnormalities, developmental delay, and connective tissue abnormalities). The described facial features include frontal bossing, dental problems, ptosis narrow palpebral fissures, and hypertelorism. Reference Thienpont1–Reference Woods, Marson and Coci5 To best of my knowledge, only couple of cases in fetal literature has been reported so far. Reference Weiss, Applegate, Wang and Batista2,Reference Gao and Li9
Case report
A 23-year-old primigravida was referred at 23 weeks gestation for fetal cardiac evaluation in view of cardiomegaly in routine obstetric scan. Four-chamber view showed cardiomegaly with thickened redundant myxomatous tricuspid and mitral valve leaflets. There was significant mitral and tricuspid valve prolapse with moderate tricuspid and mitral valve regurgitation. (Fig. 1a, b; Videoclip 1 and 2) Three-vessel view showed thickened right pulmonary artery. (Fig. 1c) Right ventricular outflow tract view showed thickened pulmonary valve (Fig. 1d, e) and bicuspid aortic valves (fusion of left and non-coronary leaflets) (Fig. 1f). High short-axis basal view of heart during diastole (Fig. 1g) and systole (Fig. 1h; Videoclip 3) showed densely thickened myxomatous tricuspid (arrow) and mitral valve leaflets (bold arrow). Invasive tests ruled out karyotype and 22q11 abnormalities. Whole exome sequencing detected a 471.5-kb deletion in the chromosome 6q25.1 (TAB2 gene). Considering the overall long-term outcome, the parents opted for termination of pregnancy. Parental whole exome sequencing and fetal autopsy were denied.
Discussion
The gene TAB2 [TGF-beta-activated kinase 1/MAP3K7-binding protein 2] mediates the activation of TAK1 in the IL-1 signal transduction pathway. TAB2 haploinsufficiency was associated with CHD. Reference Thienpont1 Up-regulation of TGF-β expression is thought to have a role in mitral valve degeneration. Variable degrees of heart defects involving the valves, outflow tract, and septum have been reported in the literature. Polyvalvular dysplasia has been reported frequently in 6q25.1 (TAB2) deletion apart from trisomy 18, Noonan, Marfan, and Ehlers-Danlos syndromes. Reference Weiss, Applegate, Wang and Batista2 A detailed literature search of various cardiac and extracardiac features of 6q25.1 (TAB2) deletion has been presented in Table 1. Reference Weiss, Applegate, Wang and Batista2-Reference Gao and Li9
Conclusion
6q25.1 (TAB2) deletion is one of the notable causes for myxomatous degeneration of cardiac valves. Whole exome sequencing must be considered in these subsets of cases for effective prenatal counselling.
Supplementary material
The supplementary material for this article can be found at https://doi.org/10.1017/S1047951123004419.
Data availability statement
Data sharing is not applicable to this article as no datasets were generated or analysed during the current study.
Financial support
This research received no specific grant from any funding agency, commercial, or not-for-profit sectors.
Competing interests
None.
Informed consent
Informed consent was obtained as per our hospital policy.