FCMR
FCMR (Familial Cardiomyopathy Registry) is a medical registry that collects data on families with a history of cardiomyopathy, a group of diseases that affect the heart muscle. The registry aims to improve understanding of these diseases, identify genetic factors that contribute to them, and develop more effective treatments.
Overview[edit | edit source]
The FCMR was established to facilitate research into the genetic causes of cardiomyopathy. It collects detailed medical and family history information from individuals who have been diagnosed with cardiomyopathy, as well as their family members. The registry is a valuable resource for researchers studying the genetic basis of these diseases.
Types of Cardiomyopathy[edit | edit source]
There are several types of cardiomyopathy, including:
- Dilated cardiomyopathy (DCM)
- Hypertrophic cardiomyopathy (HCM)
- Restrictive cardiomyopathy (RCM)
- Arrhythmogenic right ventricular cardiomyopathy (ARVC)
Each of these types affects the heart muscle in different ways and can lead to a variety of symptoms and complications, including heart failure, arrhythmia, and sudden cardiac death.
Purpose and Goals[edit | edit source]
The primary goal of the FCMR is to identify the genetic factors that contribute to the development of cardiomyopathy. By studying families with a history of these diseases, researchers hope to identify the genes that are responsible for causing them. This could lead to the development of new treatments and preventive measures.
In addition, the FCMR aims to improve the diagnosis and management of cardiomyopathy. By collecting detailed information on the symptoms, progression, and treatment of these diseases, the registry can help to inform clinical practice and improve patient outcomes.
Participation[edit | edit source]
Participation in the FCMR is voluntary and open to anyone who has been diagnosed with cardiomyopathy, as well as their family members. Participants are asked to provide detailed medical and family history information, and may also be asked to provide a blood or saliva sample for genetic testing.
See Also[edit | edit source]
References[edit | edit source]
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