Familial restrictive cardiomyopathy
अंतिम अद्यतन 30 Sept 2025
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Familial restrictive cardiomyopathy is a genetic form of heart disease. For the heart to beat normally, the heart (cardiac) muscle must contract and relax in a coordinated way. Oxygen-rich blood from the lungs travels first through the upper chambers of the heart (the atria), and then to the lower chambers of the heart (the ventricles).
विवरण
Familial restrictive cardiomyopathy is a genetic form of heart disease. For the heart to beat normally, the heart (cardiac) muscle must contract and relax in a coordinated way. Oxygen-rich blood from the lungs travels first through the upper chambers of the heart (the atria), and then to the lower chambers of the heart (the ventricles).
In people with familial restrictive cardiomyopathy, the heart muscle is stiff and cannot fully relax after each contraction. Impaired muscle relaxation causes blood to back up in the atria and lungs, which reduces the amount of blood in the ventricles.
Familial restrictive cardiomyopathy can appear anytime from childhood to adulthood. The first signs and symptoms of this condition in children are failure to gain weight and grow at the expected rate (failure to thrive), extreme tiredness (fatigue), and fainting. Children who are severely affected may also have abnormal swelling or puffiness (edema), increased blood pressure, an enlarged liver, an abnormal buildup of fluid in the abdominal cavity (ascites), and lung congestion. Some children with familial restrictive cardiomyopathy do not have any obvious signs or symptoms, but they may die suddenly due to heart failure. Without treatment, the majority of affected children survive only a few years after they are diagnosed.
Adults with familial restrictive cardiomyopathy typically first develop shortness of breath, fatigue, and a reduced ability to exercise. Some individuals have an irregular heart beat (arrhythmia) and may also experience a sensation of fluttering or pounding in the chest (palpitations) and dizziness. Abnormal blood clots are commonly seen in adults with this condition. Without treatment, approximately one-third of adults with familial restrictive cardiomyopathy do not survive more than five years after diagnosis.
Inheritance patterns
The source lists the following possible inheritance patterns: Autosomal dominant. More than one pattern can apply in different cases.
Related genes
Other names
Cardiomyopathy, restrictive
RCM
Related patient information and medicines
Patient information leaflet
विस्तारित कार्डियोमायोपैथी
Dilated cardiomyopathy is a condition where the heart muscle becomes stretched and thin. The heart becomes enlarged (dilates) and pumps blood less well. Dilated cardiomyopathy is uncommon, but it is the most common type of cardiomyopathy. Another possibility is that an unknown viral infection may be responsible. About one in four people with.
Patient information leaflet
हृदय रोग
Heart rhythm problems See the separate leaflet called Abnormal Heart Rhythms (Arrhythmias). Cardiomyopathy Cardiomyopathies are diseases that affect the heart muscle. There are several types: Hypertrophic cardiomyopathy. Dilated cardiomyopathy. Restrictive cardiomyopathy: this is a rare form of cardiomyopathy in which the heart muscle is not able.
Patient information leaflet
सारकॉइडोसिस
Heart Sarcoidosis can affect your heartbeat by making it slower या irregular. Damage to your lungs, caused ... This is known as cor pulmonale and can lead to heart failure if left untreated. Your heart can also become generally enlarged in sarcoidosis, known as cardiomyopathy. This means that your heart cannot beat as strongly or effectively and.
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हीमोक्रोमैटोसिस
Haemochromatosis symptoms Symptoms of haemochromatosis usually start between the ages of 30 and 50 years. Disease of the heart muscle (cardiomyopathy). Most of these symptoms are found in other dis... The possible complications of haemochromatosis include: Diabetes due to damage to the pancreas. हृदय disease -for example it can lead to the heart.
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हाइपरट्रॉफिक कार्डियोमायोपैथी
में हाइपरट्रॉफिक कार्डियोमायोपैथी यह heart muscle becomes thickened (hypertrophies) in parts of the heart. In the normal heart, the muscle cells are regular and patterned. Hypertrophic cardiomyopathy is a disease in which the heart muscle becomes thickened. The muscle surrounding the left ventricle is the area commonly a... How common is.
Patient information leaflet
ड्यूचेन मस्कुलर डिस्ट्रॉफी
This type of treatment has improved over recent years, which has helped to improve the quality of life and outlook for people with DMD. Heart (cardiac) complications Teenagers and adults with DMD may develop a दिल problem called कार्डियोमायोपैथी , which means weakness of the heart muscle. With DMD, the cardiomyopathy does not usually cause much in.
अधिक पठन और संदर्भ
- Familial restrictive cardiomyopathy; MedlinePlus, National Library of Medicine.
- Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, Dubourg O, Kuhl U, Maisch B, McKenna WJ, Monserrat L, Pankuweit S, Rapezzi C, Seferovic P, Tavazzi L, Keren A. Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J. 2008 Jan;29(2):270-6. doi: 10.1093/eurheartj/ehm342. Epub 2007 Oct 4.
- Kaski JP, Syrris P, Burch M, Tome-Esteban MT, Fenton M, Christiansen M, Andersen PS, Sebire N, Ashworth M, Deanfield JE, McKenna WJ, Elliott PM. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes. Heart. 2008 Nov;94(11):1478-84. doi: 10.1136/hrt.2007.134684. Epub 2008 May 8.
- Mogensen J, Arbustini E. Restrictive cardiomyopathy. Curr Opin Cardiol. 2009 May;24(3):214-20. doi: 10.1097/hco.0b013e32832a1d2e. No abstract available.
- Muchtar E, Blauwet LA, Gertz MA. Restrictive Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy. Circ Res. 2017 Sep 15;121(7):819-837. doi: 10.1161/CIRCRESAHA.117.310982.
- Nihoyannopoulos P, Dawson D. Restrictive cardiomyopathies. Eur J Echocardiogr. 2009 Dec;10(8):iii23-33. doi: 10.1093/ejechocard/jep156.
- Sen-Chowdhry S, Syrris P, McKenna WJ. Genetics of restrictive cardiomyopathy. Heart Fail Clin. 2010 Apr;6(2):179-86. doi: 10.1016/j.hfc.2009.11.005.
- Xu Q, Dewey S, Nguyen S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. J Mol Cell Cardiol. 2010 May;48(5):899-909. doi: 10.1016/j.yjmcc.2010.03.005. Epub 2010 Mar 16.
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