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H880

Dilated Cardiomyopathy (DCM) is a disorder characterised by enlargement of the heart (especially of the left ventricle), poor myocardial contractility, and congestive heart failure.

Working days 10

Specifiche

Breeds

Gene

Organ

specimen

Swab, Blood EDTA, Blood Heparin, Semen, Tissue
Mode of Inheritance

Chromosome

Also known as

Year Published

Informazioni generali

Dilated Cardiomyopathy (DCM) is a disorder characterised by enlargement of the heart (especially of the left ventricle), poor myocardial contractility, and congestive heart failure. This specific test detects a mutation located on Chromosome 5, which is one of several that is associated with the disease in the Doberman.

Caratteristiche cliniche

DCM is an enlargement of the heart that can result in decreased heart function and abnormal heart rhythm. Clinical signs of heart failure due to DCM include fainting or collapse, weight loss, breathlessness, fluid retention in the abdomen, and sudden death due to cardiac arrest.

Informazioni aggiuntive

The mutation in this test should be considered a risk factor. It is associated with the disorder, but does not necessarily guarantee it.

Riferimenti

Pubmed ID: 37723491

Omia ID: 162

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3. Risultati

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