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Right-axis deviation and anterior wall thallium-201 defect in Becker's muscular dystrophy
Ist Teil von
The American journal of cardiology, 1985-07, Vol.56 (1), p.203-204
Ort / Verlag
New York, NY: Elsevier Inc
Erscheinungsjahr
1985
Quelle
EZB-NALI5-00465 Elsevier Archive NL
Beschreibungen/Notizen
Dilated cardiomyopathy has been shown to occur in families with X-linked recessive (Becker's) muscular dystrophy.
1 Pedigree members of such families frequently manifest various electrocardiographic anomalies, including infranodal blocks (for example, left bundle branch block and complete atrioventricular block),
2–4 left-axis deviation, small Q waves in leads I and aVL and loss of R-wave amplitude in lead V
2 and V
3. Myocardial perfusion scanning in patients with early-onset, autosomal recessive muscular dystrophy has frequently shown posterobasal and lateral perfusion defects that may be a unique marker of that disorder in the heart.
5 Perfusion scanning in patients with late-onset muscular dystrophy has not been described.