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1 results

A new discovered gene mutation in a child with dilated cardiomyopathy
Part of
- Atrial Septal Defect (ASD)
- Ventricular Septal Defect (VSD)
Xiaolong Chen, Yewei Xie, Xiaobing Li, Jin Gong, Li Shen, Rufang Zhang
Journal: Cardiology in the Young / Volume 31 / Issue 9 / September 2021
Published online by Cambridge University Press: 05 April 2021, pp. 1530-1531
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Dilated cardiomyopathy is characterised by dilatation and impaired contraction of the left ventricle or both ventricles, which is the most common childhood cardiomyopathy. In recent years, it has been recognised that many sorts of genetic mutations may contribute to dilated cardiomyopathy. We now report a rare association of dilated cardiomyopathy with site mutation of BMPR2 gene. We did not find such an association reported in the medical literature.