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Q. Illustrate Hypertrophic cardiomyopathy?
It is a genetic disorder due to mutations in the gene that encodes for β-Cardiac myosin heavy chain (Localised to chromosome 14). It is characterized by inappropriate myocardial hypertrophy in absence of hypertension or aortic stenosis. There is myocardial disarray and interstitial fibrosis. It has asymmetric septal hypertrophy, left ventricular outflow obstruction due to systolic anterior motion of mitral valve, LV diastolic dysfunction, myocardial ischaemia and arrhythmias. LV outflow obstruction occurs only in about ¼th. The prevalence of HCM is about 0.2 per cent.
REDISCOVERY OF MENDEL'S LAWS (THE BIRTH OF GENETICS) 1. It was in 1900 that three botanist independently rediscovered the principles of heredity already worked out by M
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What are the events that mark the beginning and the end of the third interphase period? What happens in the cell in this period? The third interphase period is the G2. It star
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In what forms are nitrogenous wastes excreted in birds, humans and aquatic turtles respectively ? Why so, describe?
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