Genetics of Cardiovascular and Neuromuscular Disease

Launched by UNIVERSITY OF CHICAGO · Aug 29, 2005

Keywords

ClinConnect Summary

This clinical trial is focused on understanding the genetics behind certain heart and muscle diseases, specifically cardiomyopathy (a heart condition), arrhythmias (irregular heartbeats), and muscular dystrophy (a group of diseases that weaken muscles). The researchers are looking for specific genes and mutations that may cause these conditions, as some genes can lead to both heart and muscle problems when they are changed in certain ways. By studying the DNA of patients, especially those from families where multiple members are affected, the goal is to better understand how these diseases develop.

Anyone of any age with a suspected inherited heart or muscle disorder may be eligible to participate, especially families with more than one person affected by these conditions. If someone does not have a suspected genetic condition related to the heart or muscles, they will not be included in the study. Participants can expect to provide samples for genetic testing, which could provide important insights into their health and potentially help researchers develop better treatments in the future.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Patients of all ages will be considered for the study. In particular, families with more than one affected relative will be sought.
• Exclusion Criteria:
• • Subjects without a suspected inherited cardiovascular or neuromuscular disorder will be excluded from this study.