FRIEDREICH'S ATAXIA AND HYPERTROPHIC CARDIOMYOPATHY: A CASE REPORT AND REVIEW

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HANANE BENHALLA; CAMELIA SOREA

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Journal: Iranian Heart Journal Year:2015 | Volume:16 | Issue:4 Page(s): 57-59

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Information Journal Paper

Title

FRIEDREICH'S ATAXIA AND HYPERTROPHIC CARDIOMYOPATHY: A CASE REPORT AND REVIEW

Author(s)

HANANE BENHALLA | CAMELIA SOREA | Issue Writer Certificate

Keywords

FRIEDREICH'S ATAXIA

HYPERTROPHIC CARDIOMYOPATHY

FAMILIAL NEURODEGENERATIVE DISEASE

Abstract

FRIEDREICH'S ATAXIA is an autosomal recessive, spinocerebellar, degenerative disease characterized clinically by the ataxia of the limbs and trunk, dysarthria, loss of deep tendon reflexes, sensory abnormalities, skeletal deformities, diabetes mellitus, and cardiac involvement. FRIEDREICH'S ATAXIA is generally associated with concentric HYPERTROPHIC CARDIOMYOPATHY. Cardiac death occurs primarily in those developing dilated cardiomyopathy. These patients tend to do poorly with rapid progression to end-stage congestive heart failure.

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APA: Copy

HANANE, BENHALLA, & CAMELIA, SOREA. (2015). FRIEDREICH'S ATAXIA AND HYPERTROPHIC CARDIOMYOPATHY: A CASE REPORT AND REVIEW. IRANIAN HEART JOURNAL (IHJ), 16(4), 57-59. SID. https://sid.ir/paper/279734/en

Vancouver: Copy

HANANE BENHALLA, CAMELIA SOREA. FRIEDREICH'S ATAXIA AND HYPERTROPHIC CARDIOMYOPATHY: A CASE REPORT AND REVIEW. IRANIAN HEART JOURNAL (IHJ)[Internet]. 2015;16(4):57-59. Available from: https://sid.ir/paper/279734/en

IEEE: Copy

BENHALLA HANANE, and SOREA CAMELIA, “FRIEDREICH'S ATAXIA AND HYPERTROPHIC CARDIOMYOPATHY: A CASE REPORT AND REVIEW,” IRANIAN HEART JOURNAL (IHJ), vol. 16, no. 4, pp. 57–59, 2015, [Online]. Available: https://sid.ir/paper/279734/en

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