medigraphic.com
SPANISH

Correo Científico Médico de Holguín

ISSN 1560-4381 (Print)
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2012, Number 4

<< Back Next >>

Correo Científico Médico 2012; 16 (4)

Presentation of a Patient with Hypertrophic Cardiomyopathy

Gonzalez FMA González GV, Piriz ACA
Full text How to cite this article

Language: Spanish
References: 4
Page:
PDF size: 149.66 Kb.


Key words:

gene mutation, cardiomyopathy, hypertrophy, sudden death, myocardial ischemia.

ABSTRACT

A 16- year- old female patient with hypertrophic cardiomyopathy diagnosed 12 days after birth was presented in this paper. This is a genetic autosomal dominant inheritance disease characterized by increased muscle mass and myofibrillar disarray with high risk of sudden death, which has no racial or ethnic bias. It has a prevalence of 1 / 500 families. Affected patients usually have abnormal intramural coronary arteries, and the dynamic pressure gradient across the outflow tract of the left ventricle is the most representative of this disease.The degree of obstruction varies from patient to patient.


REFERENCES

  1. 1 Jiménez Casso MS, Benito BF. Miocardiopatía hipertrófica. Protocolos de cardiopediatría. [citado 24 nov 2011]. Disponible en: http://www.secardioped.org/Descargas/PyB/LP_cap45.pdf

  2. 2 Miyake C.Y, Berul C. Hypertrophic Cardiomyopathy [citado 24 nov 2011]. Disponible en: http://emedicine.medscape.com/article/890068-overview

  3. 3 Navarro López F. Miocardiopatía hipertrófica. Bases genéticas e implicaciones clínicas. Rev Esp Cardiol. 2004; 57:22-32.

  4. 4 Zarco P. Devenir conceptual de la miocardiopatía hipertrofica. Monocardio. 2000;(2)2:1-4.




2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Correo Científico Médico. 2012;16