Restrictive cardiomyopathy

Restrictive cardiomyopathy

Infobox_Disease
Name = PAGENAME


Caption =
DiseasesDB = 11390
ICD10 = ICD10|I|42|5|i|30
ICD9 = ICD9|425.4
ICDO =
OMIM =
MedlinePlus = 000189
eMedicineSubj = med
eMedicineTopic = 291
MeshID = D002313

Restrictive cardiomyopathy (RCM) is the least common cardiomyopathy. It is called this because it restricts the heart from stretching and filling with blood properly. Rhythmicity and contractility of the heart may be normal, but the stiff walls of the heart chambers (atria and ventricles) keep them from adequately filling. So blood flow is reduced, and blood that would normally enter the heart is backed up in the circulatory system. In time, restrictive cardiomyopathy patients develop diastolic dysfunction and eventually heart failure.

Common causes include haemochromatosis, amyloidosis, sarcoidosis, postradiation fibrosis, endocardial fibroelastosis, connective tissue diseases (scleroderma) and Löffler's syndrome.

Therapy for restrictive cardiomyopathy is limited. Diuretics may help relieve symptoms.

External links

* [http://www.merck.com/mmhe/sec03/ch026/ch026d.html Overview] at Merck Manual


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