[引用][C] Noncompaction in myotonic dystrophy type 1 on cardiac MRI
J Finsterer, C Stöllberger, W Kopsa - Cardiology, 2005 - karger.com
J Finsterer, C Stöllberger, W Kopsa
Cardiology, 2005•karger.comThe number of CTG repeats in the myotonic dystrophy protein kinase gene on chromosome
19q13. 3 was 5 for the normal allele and 300 for the expanded allele. The daughter of the
patient was clinically unaffected, but carried an expanded allele as well. Except for atrial
flutter, which was successfully converted into sinus rhythm, no Left ventricular
hypertrabeculation/noncompaction (LVHT) is a rare subtype of hypertrophic
cardiomyopathy, affecting the left ventricular myocardium distal to the papillary muscles [1] …
19q13. 3 was 5 for the normal allele and 300 for the expanded allele. The daughter of the
patient was clinically unaffected, but carried an expanded allele as well. Except for atrial
flutter, which was successfully converted into sinus rhythm, no Left ventricular
hypertrabeculation/noncompaction (LVHT) is a rare subtype of hypertrophic
cardiomyopathy, affecting the left ventricular myocardium distal to the papillary muscles [1] …
The number of CTG repeats in the myotonic dystrophy protein kinase gene on chromosome 19q13. 3 was 5 for the normal allele and 300 for the expanded allele. The daughter of the patient was clinically unaffected, but carried an expanded allele as well. Except for atrial flutter, which was successfully converted into sinus rhythm, no
Left ventricular hypertrabeculation/noncompaction (LVHT) is a rare subtype of hypertrophic cardiomyopathy, affecting the left ventricular myocardium distal to the papillary muscles [1]. LVHT is frequently associated with neuromuscular disorders [2, 3]. LVHT has not been described on cardiac MRI in myotonic dystrophy type 1 (MD1).
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