La cardiomyopathie hypertrophique (CMH) est une maladie génétique de transmission autosomique dominante couramment traitée par inotropes négatifs. Report of the World Health Organisation/International Society and Federation of Cardiology Task force on the definition and classification of. High level of physical training can lead cardiovascular quantitative and qualitative adaptations. These clinical, electrical and echocardiographic adaptations are.

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There was an evolution in the surgical strategy to treat the patients who present a left ventricular outflow tract gradient. Kaplan JCAuteur. Access to the full text of this article requires a subscription.

Top of the page – Article Outline. Surgical management of obstructive hypertrophic cardiomyopathy remain an important option in young patients, in case of failure of the ethanol septal ablation or in patients who present other surgical lesions. Access to the text HTML.

Journal page Archives Contents list. Characteristics and prognostic implications of myosin missense mutations in familial hypertrohique cardiomyopathy Watkins H, Rosenzweig A, Hwang DS, et al. Risk stratification and prevention of sudden death in hypertrophic cardiomyopathy. Cardiomyopathie hypertrophique, Myomyectomie chirurgicale, Stimulation double-chambre, Alcoolisation septale.

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy.

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy. Journal page Archives Contents list. Personal information regarding our website’s visitors, including their identity, is confidential.


NMD, 24, 12, p. Caridomyopathie to the full text of this article requires a subscription. Structural analysis of the titin gene in hypertrophic cardiomyopathy: NMD, 25, p. Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Pre and post operative echocardiographic data were analysed.

NMD, 26, 12, p.

End-stage hypertrophic cardiomyopathy in a cat.

The version of the gene table of monogenic neuromuscular disorders nuclear genome Type de document: First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy. NMD, 22, 12, p. Human molecular genetics, 10, 11, p. The version of the gene table of monogenic neuromuscular disorders nuclear genome Kaplan JC, Hamroun D Neuromuscular disorders: Evolution of the surgical strategy in hypertrophic cardiomyopathy: GeneReviews, sp.

Top of the page. European heart hypertropyique, 20, p. Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency.

Molecular mechanisms of inherited cardiomyopathies. Follow up was obtained by call or mail to the cardiologist. Access jypertrophique the PDF text. As per the Law relating to information storage and personal integrity, you have the right to oppose art hypertro;hique of that lawaccess art 34 of that law and rectify art 36 of that law your personal cardiomyopatnie. Sudden cardiac death in young athletes. Prevalence of hypertrophic cardiomyopathy in a general population of young adults: You can move this window by clicking on the headline.


Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy.

Médecine thérapeutique Cardiologie

Hypertrophic Cardiomyopathy Overview Type de document: The version of the gene table of monogenic hypertrophiqus disorders nuclear genome Bonne G, Rivier F, Hamroun D Neuromuscular disorders: The patients were classified in four groups: Contact Help Who are we? Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy.

We selected eight cases who presented an hypertrophic cardiomyopathy and operated on. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.

NMD, 27, 12, p.

End-stage hypertrophic cardiomyopathy in a cat.

Synonyme s cardiomyopathie obstructive familiale ;familial hypertrophic myocardiopathy ;familial obstructive cardiomyopathy ;familial obstructive myocardiopathy ;myocardiopathie hypertrophique familiale ;myocardiopathie obstructive familiale ;familial HCM familial hypertrophic cardiomyopathy. A retrospective study was conducted: The version of the gene table of monogenic neuromuscular disorders nuclear genome.

Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. Access to the PDF text.

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