cardiovascular system
• exhibit myofiber disarray in hearts
|
• markers of hypertrophy are elevated
|
• develop left ventricle (LV) hypertrophy, with an increase in maximal LV wall thickness and a reduction in LV end-diastolic diameter
|
• exhibit prolongation of the PR interval, consistent with first-degree atrioventricular block
|
• exhibit decreased QRS and QRS-H
|
• cardiomyocytes exhibit abnormal calcium cycling with a prolonged decay constant in calcium transients and a reduced decay constant in response to caffeine treatment, however show normal sarcoplasmic reticulum calcium release and storage
|
• develop hallmarks of familial hypertrophic cardiomyopathy by 21 weeks of age
|
muscle
• exhibit myofiber disarray in hearts
|
• develop left ventricle (LV) hypertrophy, with an increase in maximal LV wall thickness and a reduction in LV end-diastolic diameter
|
• develop hallmarks of familial hypertrophic cardiomyopathy by 21 weeks of age
|
growth/size/body
• markers of hypertrophy are elevated
|
• develop left ventricle (LV) hypertrophy, with an increase in maximal LV wall thickness and a reduction in LV end-diastolic diameter
|
cellular
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
hypertrophic cardiomyopathy 7 | DOID:0110313 |
OMIM:613690 |
J:114537 |