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ATTR Gene Variants in HCM.
Kanelidis, Anthony J; Slivnick, Jeremy A; Campagna, Rachel; Smith, Bryan; Kalantari, Sara; Sarswat, Nitasha; Kim, Gene.
Affiliation
  • Kanelidis AJ; University of Chicago Medicine, Chicago, Illinois, USA.
  • Slivnick JA; University of Chicago Medicine, Chicago, Illinois, USA.
  • Campagna R; University of Chicago Medicine, Chicago, Illinois, USA.
  • Smith B; University of Chicago Medicine, Chicago, Illinois, USA.
  • Kalantari S; University of Chicago Medicine, Chicago, Illinois, USA.
  • Sarswat N; University of Chicago Medicine, Chicago, Illinois, USA.
  • Kim G; University of Chicago Medicine, Chicago, Illinois, USA.
JACC Case Rep ; 29(6): 102236, 2024 Mar 20.
Article in En | MEDLINE | ID: mdl-38549855
ABSTRACT
Hypertrophic cardiomyopathy is the most common inherited cardiomyopathy, with a prevalence of 1200 to 1500. Cardiac amyloidosis, another cardiomyopathy caused by myocardial deposition of abnormally folded TTR protein, can be acquired or hereditary. The presence of pathogenic TTR gene variants in patients with phenotypic HCM is an underrecognized and clinically important entity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JACC Case Rep Year: 2024 Document type: Article Affiliation country: United States Country of publication: Netherlands
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JACC Case Rep Year: 2024 Document type: Article Affiliation country: United States Country of publication: Netherlands