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37 Cards in this Set
- Front
- Back
hypertensive heart disease
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increased afterload that results in hypertrophy and greater metabolic req
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cor pulmonale
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right sided heart disease as a result of pumlonary hypertension
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pulmonary hypertension
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elevated blood pressure in the pulmonary circuit
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chronic cor pulmonare
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cuased by disease of the lungs, ulmonary vessels, restricted chest movement, and [processes cuasing pulmonary arteriolar constriction
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rheumatic heart disease
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cross reactivity between heart and M proteins in the cells walls of cetain strep
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mitral valve prolapse
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due to floppy mitral valve one or both cusps evert during systole
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cardiomyopahty
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primary disease of the myocardium
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ventricular septal defect
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allows blood to flow from l ventricle back to right
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root of the aorta overrides the septal defect
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soem of blood enering the body is not oxygenated
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insulin
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anabolic hormone
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glucose tolerance test
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75 grams and two hour plasma glucose of 200 mg/dl
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polydipsia
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drink a lot
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polyuria
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urinate a lot
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polyphagia
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eat a lot
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insulin resistance
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the inability of insulin to act effectively on target tissues lik the muscle and liver
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cushing's syndrome
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exess cortisol production
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acromegaly
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excess growth hormone
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pheochromocytoma
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tumor of the adrenal medulla dumps excess catecholamines
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long term evaluation
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elevated glucose over prolonged periods causes an increase in enzymatic glycoslation of hemoglobin
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pyelonephritis
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an acute or chronic inflammation of the kidney tubules and interstitial tissue usually dues to porr circulation or bacterial infection
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diabetic retinopathy
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retinal blood vessels leak plasma into the retina which si toxic to the retina
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diabetic neuropathy
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direct axonal damage fromt he altered metabolism
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point mutation
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substitution of a single nucelotide base with another
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missense mutation
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REPLACEMENT OF ONE AMINO ACID WITH ANOTHER ASSOCIATED WITH APOINT MUTATION
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nonsense codon
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replacement of an amino acid wiht astop codon
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trinucleotide repeat mutation
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amplification of a specific set of 3 nucleotide seuences within a gene disrupts its fuction
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frameshift mutaiton
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a single base is deleted resulting in a change in transcription of all subsequent aa
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three base deletion
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results in the los of an aa
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penetrance
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soem indiidual inherit the disease but are phenotypically normal as in autosomal dominant disease
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expressivity
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manifest the disease more seriously than others like in autosomla dominant diseases
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regurgitation
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mitral valve prolapse and leakage
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hemathroses
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bleed into joints
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intestinal stenosis
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small lumen
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klnefelter's synbdrome
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XXY males
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gynecomastia
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breat development in males
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turnor syndrome
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XO female
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bastoma
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cancer of a germ cell
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