Pathogenic variant of RBM20 in a multiplex family with hypertrophic cardiomyopathy
RBM20 is a disease-causing gene associated with dilated cardiomyopathy (DCM). The proband presented with the dilated phase of hypertrophic cardiomyopathy (HCM), and the mother also suffered from HCM. A missense variant of RBM20 , p.Arg636His, previously reported as pathogenic in several families wit...
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Veröffentlicht in: | Human genome variation 2022-02, Vol.9 (1), p.6-6, Article 6 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | RBM20
is a disease-causing gene associated with dilated cardiomyopathy (DCM). The proband presented with the dilated phase of hypertrophic cardiomyopathy (HCM), and the mother also suffered from HCM. A missense variant of
RBM20
, p.Arg636His, previously reported as pathogenic in several families with DCM, was found in both the proband and the mother. Therefore,
RBM20
p.Arg636His could be the causative variant for this familial HCM, and
RBM20
might be a novel causative gene for HCM. |
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ISSN: | 2054-345X 2054-345X |
DOI: | 10.1038/s41439-022-00183-z |