Hypertrophic cardiomyopathy causes
Hypertrophic Cardiomyopathy Microchapters
Hypertrophic cardiomyopathy causes On the Web
Hypertrophic cardiomyopathy is a condition that is most often passed down through families (inherited). It is thought to result from gene mutations that control heart muscle growth. Genes involved in the pathogenesis of hypertrophic cardiomyopathy include MYH7, TNNT2, TPM1. Nevertheless, a number of chronic medical conditions might be contributed to hypertrophic cardiomyopathy development, among them are thyroid disease, diabetes, and obesity, and hypertension.
Life Threatening Causes
Life-threatening causes include conditions that may result in death or permanent disability within 24 hours if left untreated.
Causes by Organ System
Causes in Alphabetical Order
- Atrial myxoma
- Cardiofaciocutaneous syndrome
- Congenital generalized lipodystrophy type 2
- Costello syndrome 
- Cytochrome c oxidase deficiency
- Diabetes mellitus
- Dihydrolipoamide dehydrogenase deficiency
- Fabry's disease
- Friedreich's ataxia
- Gene mutation
- Glycogenosis type 2
- Hereditary spherocytosis
- Hypertrichotic osteochondrodysplasia
- Hypertrophic obstructive cardiomyopathy
- Long-chain acyl-CoA dehydrogenase deficiency
- Malonyl-CoA decarboxylase deficiency
- Multiple lentigines syndrome
- Muscle glycogen synthase deficiency
- Myotonic dystrophy
- Noonan syndrome
- Sarcomeric protein mutations
- Subendocardial ischemia
- Thyroid disease
- Very long-chain acyl-CoA dehydrogenase deficiency
- Yunis-Varon syndrome
Hypertrophic cardiomyopathy is transmitted in an autosomal dominant pattern.
The development of Hypertrophic cardiomyopathy is the result of multiple genetic mutations such as:
HCM is the most common genetically transmitted cardiovascular disease. Hypertrophic cardiomyopathy is inherited as an autosomal dominant trait and is attributed to mutations in one of a number of genes that encode for one of the sarcomere proteins. Penetrance of HCM is incomplete, variable and time or age-related. The disease may be sporadic but affected family members are discovered in 13% of cases. More than 200 mutations involving at least 10 chromosomes encoding structural proteins of the myocyte have been discovered. These mutations have varying degrees of penetrance and even the same mutation may have variable expression, implying the superimposed effects of other genes or environmental influences. Children of a patient with HCM have a 50% chance of inheriting the trait.
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- Fukao T, Sakai S, Shimozawa N, Kuwahara T, Kano M, Goto E; et al. (1996). "Life-threatening cardiac involvement throughout life in a case of Costello syndrome". Clin Genet. 50 (4): 244–7. PMID 9001809.
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- Jauslin ML, Wirth T, Meier T, Schoumacher F (2002). "A cellular model for Friedreich Ataxia reveals small-molecule glutathione peroxidase mimetics as novel treatment strategy". Hum Mol Genet. 11 (24): 3055–63. PMID 12417527.
- Halawa A, Iskandar SB, Brahmbhatt V, Fahrig SA (2007). "Atrial flutter and myotonic dystrophy in a male adolescent treated with radiofrequency catheter ablation". Rev Cardiovasc Med. 8 (2): 118–22. PMID 17603429.
- Prendiville TW, Gauvreau K, Tworog-Dube E, Patkin L, Kucherlapati RS, Roberts AE; et al. (2014). "Cardiovascular disease in Noonan syndrome". Arch Dis Child. 99 (7): 629–34. doi:10.1136/archdischild-2013-305047. PMID 24534818.
- Tucci S, Flögel U, Hermann S, Sturm M, Schäfers M, Spiekerkoetter U (2014). "Development and pathomechanisms of cardiomyopathy in very long-chain acyl-CoA dehydrogenase deficient (VLCAD(-/-)) mice". Biochim Biophys Acta. 1842 (5): 677–85. doi:10.1016/j.bbadis.2014.02.001. PMID 24530811.