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37 Cards in this Set

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