Rare heart disease causes are not well understood and even in present – modern – times we still dont know the root causes of some of these rare heart muscle diseases. What we do know is that many of these problems are life threatening and that, through observation, doctors have gathered a list of symptoms of heart diseases and ways to effectively apply reverse heart disease treatments to afflicted patients.

Here are a few of the rare heart muscle diseases and some information about them. Always remember to visit your doctor regularly or at least once a year for a complete checkup.

Abetalipoproteinemia is a recessive disorder that is characterized by the lack of a protein B-containing lipo proteins from plasma. The irregular absorption of fat tissue is severe and triglyceride accumulation occurs. Another disease called Acanthocytosis in which the majority of red blood cells will develop multiple spiny cytoplasmic projections can be a common occurrence due to the presence of Abetalipoproteinemia.

Anti-phospholipid Syndrome or APS is characterized by the presence of circulating auto antibodies to certain lipids containing phosphorus. It’s clinical manifestation can be observed in recurrent blood clotting, repeated fetal deaths, and auto immune diseases like thrombocytopenia.

Beta-sitosterolemia is a very rare congenital error of the metabolism that is characterized by an increased absorption of the dietary cholesterol and plant and shellfish sterols, where patients with this disease will have a marked increase in the risk of premature cardiovascular diseases. No Effective treatment is available at present times although there are a number of medical compounds and drugs with studies underway.

Brugadas syndrome is another rare inherited disease in which cardiac electro physiological abnormalities are found in patients. Right bundle branch blocks and ST elevation in the precordial leads are the most common manifestations, and it is associated with a very high frequency of sudden cardiac death.

DiGeorge syndrome is characterized by many abnormalities in new born babies including cardiac outflow tract abnormalities, cleft palate, facial dysmorphogenesis, hypoplasia of the thymus and parathyroid glands, learning difficulties, and other neuro development problems. It’s usually sporadic but also may be inherited. It’s caused by a deletion of the segment in chromosome 22.

Dysbetalipoproteinemia is a disease with a strong tradition of heritage meaning it will be passed on from one generation to the other. It is characterized by the presence of beta migrating low density lipoproteins. This disorder can lead to the formation of yellow skin plaques called xanthomas which is very characteristic, and predisposes individuals who are affected to early ischemic heart diseases.

Niemann-Pick Type C Disease is an autosomal recessive lipid-storage problem that is characterized by an excess in the accumulation of cholesterol in the spleen, liver, and other mayor organs in the body. Patients experience cardiovascular disease, enlarged liver and spleen and a severe neurological dysfunction.

These are just some of the more common rare heart disease causes, but there are others even more strange and misunderstood diseases that hopefully science will discover a reverse heart disease treatment for afflicted patients in the future.

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