ANSWERS TO QUESTIONS
*)- W^dad\nd[Y^hZVhZ
cavity. Bleeding episodes can be managed by injections of purified
Factor VIII, the antihemophilia factor.
CHAPTER 14
- d
- b
- b
- Blood pressure sphygmomanometer
Bundle of His Purkinje fibers
Coronary arteries myocardium infarction
Pericardial diseases aspirin, ibuprofen
Palpitations ventricular tachycardia
Right ventricle tricuspid valve
SA node pacemaker
Thrombolysis tenecteplase
Vasodilation lowered blood pressure
Xanthoma familial hypercholesterolemia - The changes in the normal production of adrenaline lead to
arrhythmias. - It is likely that Barry has had a myocardial infarction. However,
his chest pain has only lasted for 30 min so he will not show any
abnormal enzyme or protein levels, therefore there is no need to
investigate serum enzyme levels at this stage. - Lowering the amount of carbohydrate in the diet may decrease
triacylglycerol and cholesterol levels, because the triacylglycerols in
the VLDL particles are synthesized by the liver mainly from dietary
carbohydrate. The VLDL particle secreted into the blood will, of
course, carry cholesterol. - LDL receptors recognize ApoB-100, whereas chylomicrons contain
ApoB-48, apoC and apoE that are not recognized by LDL receptors.
CHAPTER 15
- b
- e
- 25%
- The children have equal chances of receiving the stable or mutant
gene. Fifty percent of female children will be affected. Most of the
males who receive the mutation will have the full mutation. However,
there have been cases which the number of repeats was reduced. - In autosomal dominant syndromes an affected father would pass it on
to an average of 50% of his sons and daughters. X-linked dominant
syndromes do not show male-to-male transmission but all the
daughters of an affected father would show the syndrome. If many
families were studied, the ratios of affected males to females for an
autosomal dominant would be 1:1, but 1:2 for X-linked dominant
syndromes since males have only half the chance of inheriting a
defective X chromosome. - (A) Turner (X0), (B) XYY and (C) Klinefelter (XXY) syndromes.