Registry and Prevalence of Gene Mutation in Korean Patients With Familial Hypertrophic Cardiomyopathy

Yonsei University

Status: Completed

Conditions: Familial Hypertrophic Cardiomyopathy

Study type: Observational

Funder types: Other

Identifiers

NCT01792960

4-2012-0869

Details and patient eligibility

About

Set the Korean Familial Hypertrophic Cardiomyopathy (KFHC) registry to study the prevalence of gene mutations in Korean patients with familial hypertrophic cardiomyopathy

Enrollment: 99 patients

Sex: All

Ages: 13+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. left ventricular maximal wall thickness ≥ 15mm on echocardiography
2. hypertrophic cardiomyopathy patients' relatives

Exclusion criteria

1. other cardiomyopathy or systemic disease (e.g. fabry disease, danon disease, glycogen storage disease)
2. who deny the study entrance, especially in patients' relatives

Trial design

99 participants in 1 patient group

familial hypertrophic cardiomyopathy

Description:

familial hypertrophic cardiomyopathy patients and their relatives