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-genetic disease -Affects organs that secrete mucin, tears, sweat, digestive juices, and saliva -abnormal chloride transport- results in thick mucus |
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Infection of the alveoli of the lung resulting in swelling and reduced capacity for gas exchange |
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hypersensitivity of conducting pathways leads to inflamation and bronchoconstriction |
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cigarette smoking -3 types: squamos cell carcinoma, adenocarcinoma, small cell carcinoma treatment: removal of diseased lung |
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stomach pushes through esophageal hiatus (through the diaphram) |
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Gastroesophageal reflux disease (GERD) |
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-abnormal relaxation of weakening of cardiac sphinchter -gastric reflux erodes esophageal tissue |
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erosion of stomach or duodenal mucosa *helicobacter pylori-most common cause of ulcer |
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-any hinderance to the movement of chyme of feces through intestine |
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inflammatory bowel disease |
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-periodic inflammation of intestinal wall -symptoms include cramping, diaheria, weight loss, intestinal bleeding |
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-inflammation of liver -Flu like symptoms and jaundice |
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urinary tract infection (UTI) |
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Definition
-sexually active young women -bacteria from vagina enter urethra -inflamtaion of urethra (urethritis) -bladder infection (cystitis) -kidney infection (pyelonephritis) symptoms -dysuria (painful urination), urgency, pressure in pelvis |
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approximately 4000 deaths per year -HPV infection -pap smear= test to detect Cerv. cancer -treatement -cone biopsy -hysterectomy -development of HPV vaccine? |
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normally occurs between ages 45 and 55 -cessation of ovulation and menstration -circulation lvls of estrogen and progesterone decline -reduction in uterine and breast size -bone mass decline-osteoporosis |
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Benign prostate hyperplasia (BPH) |
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Definition
noncancerous enlargement of the prostate -very common 90% of men over 80 -symptoms: nocturia, polyuria, dysuria |
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risk increases with age detected by digital rectal exam or PSA test |
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individual with both male and female sex charac. true hermaphrodites have both ovarian and testicular structures and ambiguous external genetalia |
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individual whose genetic sex and phenotypic sex do not match |
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Trisomy 21 nondisjuntion incidence increases greatly with mother's age |
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tubal pregnancy oocyte implants in uterine tube -U. tube unable to expand as fetus develops -no treatment to save baby |
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Fetal alcohol syndrome (FAS) |
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one of a few preventabel birth dfects -single binge can be a teratogen -FAS= growth retardation, heart defects, microcephally (small brain), mental retardation |
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only used as last resort for cases of extreme acne -25% of babies born to mothers on it have birth defect, 50% are mentally disabled |
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-caused by vitamin C definciency -normal collagen fibers cannot be formed -weakening of gums, teeth, and internal mucosa -prevelant amung sailors |
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-genetic disease, abnormal gene on chromosom 15 -abnormalities in fibrillin, collagen, and elasticin -causes skeletal, cardio, and connective tissue abnor. -tall and thin with long arms, toes, fingers -typically die by age 50 because of heart weakness |
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genetic and hormonal -genetic: 2 alleles one for uniform is recessive to dominant gene for baldness -hormonal: testosterone causes terminal hair to be replaced by vellus hair |
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1. fracture hematoma forms 2. soft callus forms 3. hard callus forms 4. bone remodeled |
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-soft bones in children -leads to bowed legs -vitamin D deficiency -calcium deficiency |
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excessive bone resorption aged and post-menopause |
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rupture of the annulus firbrosus leading to protrusion of nucleus pulposus -pressure on nerve and roots -treatment: NSAIDS, steroid, PT, surgery |
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Polydactyly Meromelia Phocomelia |
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Definition
-extra digits -Partial absence of a limb -short poorly formed limb (fin like) |
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inflamatory disease that damages the joints -gouty |
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autoimmune disease chronic inflammatory disorder |
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chronic pain and extreme fatigue and depression |
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Myofascial pain syndrome (MPS) |
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associated with excessive use of postural muscles |
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-inherited group of muscle disorders -muscles enlarge, though muscle fibers atrophy -most common and serious form= duchenne -x linked recessive gene -1 in 3500 births, mostly male -lacks protein called dystrophin |
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