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Feline hypertrophic cardiomyopathy (HCM) is the most common heart disease in domestic cats; [69] [70] [71] the disease process and genetics are believed to be similar to the disease in humans. [72] In Maine Coon cats, HCM has been confirmed as an autosomal dominant inherited trait. [73] Numerous cat breeds have HCM as a problem in the breed. [74]
Feline arterial thromboembolism (FATE syndrome) (German: Feline arterielle Thromboembolie) is a disease of the domestic cat in which blood clots (thrombi) block arteries, causing severe circulatory problems. Relative to the total number of feline patients, the disease is rare, but relatively common in cats with heart disease: about one-sixth of ...
Chromosomal Mutation. Cri du chat syndrome is a rare genetic disorder due to a partial chromosome deletion on chromosome 5. [1] Its name is a French term ("cat-cry" or "call of the cat") referring to the characteristic cat-like cry of affected children (sound sample [1]). [2] It was first described by Jérôme Lejeune in 1963. [3]
Holt–Oram syndrome (also called atrio-digital syndrome, atriodigital dysplasia, cardiac-limb syndrome, heart-hand syndrome type 1, HOS, ventriculo-radial syndrome) is an autosomal dominant disorder that affects bones in the arms and hands (the upper limbs) and often causes heart problems. [1] The syndrome may include an absent radial bone in ...
[2] [3] Thus the heart is restricted from stretching and filling with blood properly. It is the least common of the three original subtypes of cardiomyopathy: hypertrophic, dilated, and restrictive. [1] It should not be confused with constrictive pericarditis, a disease which presents similarly but is very different in treatment and prognosis. [1]
First reported in 1980 by J. Tuttle in a scientific article, feline hyperesthesia syndrome, also known as rolling skin disease, is a complex and poorly understood syndrome that can affect domestic cats of any age, breed, and sex. [1][2][3][4][5] The syndrome may also be referred to as feline hyperaesthesia syndrome, apparent neuritis, atypical ...
Arrhythmogenic cardiomyopathy (ACM) is an inherited heart disease. [ 1 ] ACM is caused by genetic defects of parts of the cardiac muscle known as desmosomes, areas on the surface of muscle cells which link them together. The desmosomes are composed of several proteins, and many of those proteins can have harmful mutations.
Atrioventricular septal defect (AVSD) or atrioventricular canal defect (AVCD), also known as " common atrioventricular canal " or " endocardial cushion defect " (ECD), is characterized by a deficiency of the atrioventricular septum of the heart that creates connections between all four of its chambers. It is a very specific combination of 3 ...