Left ventricular hypertrabeculation/noncompaction with PMP22 duplication-based charcot-marie-tooth disease type 1A

Cardiology

Volumn 105, Issue 3, 2006, Pages 142-145

  Corrado, Giovanni ^a   Checcarelli, Nicoletta ^a   Santarone, Mauro ^a   Stöllberger, Claudia ^b   Finsterer, Josef ^b  

^a VALDUCE HOSPITAL   (Italy)

^b KRANKENANSTALT RUDOLFSTIFTUNG   (Austria)

Author keywords

Cardiomyopathy, hypertrophic; Heart disease; Hereditary cardiac involvement; Neuropathy; Trabeculation, abnormal

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 17P; COMORBIDITY; FEMALE; GENE DUPLICATION; HEART ARRHYTHMIA; HEART DISEASE; HEART LEFT BUNDLE BRANCH BLOCK; HEART LEFT VENTRICLE HYPERTROPHY; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; NEUROPATHY; PRIORITY JOURNAL; THORAX PAIN; TRANSTHORACIC ECHOCARDIOGRAPHY;

BUNDLE-BRANCH BLOCK; CARDIOMYOPATHY, DILATED; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENE DUPLICATION; GENETIC PREDISPOSITION TO DISEASE; HEART FAILURE, CONGESTIVE; HEART RATE; HUMANS; HYPERTROPHY, LEFT VENTRICULAR; MIDDLE AGED; MYELIN PROTEINS; STROKE VOLUME;

EID: 33645473866     PISSN: 00086312     EISSN: None     Source Type: Journal    
DOI: 10.1159/000091152     Document Type: Article

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