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Familial Hypertrophic Cardiomyopathy

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Familial Hypertrophic Cardiomyopathy" returned 4 free, full-text review articles. First few results:
Multi-scale computational models of familial hypertrophic cardiomyopathy: genotype to phenotype.
Last Updated: Nov 13, 2018

Familial hypertrophic cardiomyopathy (FHC) is an inherited disorder affecting roughly one in 500 people. Its hallmark is abnormal thickening of the ventricular wall, leading to serious complications that include heart failure and sudden cardiac death. Treatment is complicated by variation ...

The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
Last Updated: Apr 06, 2011

Hypertrophic cardiomyopathy (HCM) is a familial disorder characterized by left ventricular hypertrophy in the absence of other cardiac or systemic disease likely to cause this hypertrophy. HCM is considered a disease of the sarcomere as most causal mutations are identified in genes ...

Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics.
Last Updated: Oct 25, 2016

Familial hypertrophic cardiomyopathies (FHC) are the most common genetic heart diseases in the United States, affecting nearly 1 in 500 people. Manifesting as increased cardiac wall thickness, this autosomal dominant disease goes mainly unnoticed as most affected individuals are asymptomatic. ...

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4 Free Review Articles 23 Review Articles

Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Familial Hypertrophic Cardiomyopathy" returned 4 free, full-text editorial articles. First few results:
Full PubMed Editorials matches at NCBI:
4 Free Editorials 12 Editorials

Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Familial Hypertrophic Cardiomyopathy" returned 113 free, full-text research articles. First few results:
Familial evaluation reveals a distinct genetic cause in a large Spanish family with neurofibromatosis 1 and hypertrophic cardiomyopathy.
Last Updated: May 18, 2020

Neurofibromatosis 1 (NF1) is an autosomal dominant disorder characterized by café-au-lait spots, intertriginous freckling, and multiple neurofibromas. Classically, it has been described that hypertrophic cardiomyopathy (HCM) may be a cardiovascular manifestation of neurofibromatosis ...

Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.
Last Updated: Mar 30, 2020

β‑myosin heavy chain (MHC) 7 (MYH7) is the dominant pathogenic gene that harbors mutations in 20‑30% of cases of familial hypertrophic cardiomyopathy (HCM). The aim of this study was to elucidate the distribution and type of genetic variations among Chinese HCM families. From ...

[Gene screening and phenotype analysis in a pedigree with familial hypertrophic cardiomyopathy from Yunnan Province].
Last Updated: Feb 15, 2019

To identify the disease-causing mutations in a pedigree with familial hypertrophic cardiomyopathy (HCM) from Yunnan province, and analyze the relationship between the genotype and the phenotype. The blood samples and the clinical data of the HCM family members were collected.The ...

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113 Free Research Articles 256 Research Articles