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29 Cards in this Set
- Front
- Back
opportunistic infections in AIDS
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pneumocystitis, CMV, Cryptococcus, MAI, TB, Herpes(esophagitis)
Candida(thrush, esophagitis) Cryptosporidium( acid fast, diarrhea) |
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Cocaine MOA
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decreased uptake of DOPA and NOR
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most common cause of monoclonal elecrtophoresis
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monoclonal gammopathy of undetermined significance
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UVB light
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produces thymine dimers, need to be replaced by DNA repair enzymes to prevent cancer
absent in xeroderma pigmentosum |
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ESR increase with age
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probably abnormal and indicates a disease
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key elements in wound healing
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granulation tissue and fibronectin
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cytochrome oxidase inhibited by
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CO and CN-
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Chronic granulomatous disease of childhood
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XR
absent NADPH oxidase and respiratory burst cant kill S. aureus (catalase positive) but can kill strep (catalase negative) |
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?
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coagulation necrosis in MI
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Mosaicism
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non-disjunction in somatic cells
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MC of vitamin deficiency in alcoholics
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folate
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MC of metal deficiency in alcoholics
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magnesium
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vitamin associated with pyruvate dehydrogenase
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thiamine
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respiratory burst
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NADPH oxidase conversion of molecular oxygen into superoxide free radicals
Only in neutrophils and monocytes |
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Clear cell adenocarcinoma of vagina
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DES exposure; vaginal adenosis is the precursor
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Vitamin E toxicity
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decreases levels of the vitamin K dependent factors, increases incidence of hemorrhagic strokes, potentiates the action of warfarin
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Biotin reaction
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carboxylase reaction in the conversion of pyruvate to oxalacetate
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Pyridoxine B6 involved in
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transamination of reactions involving trasaminases ALT and AST
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functions of ANP
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inhibits ADH, inhibits ATII effect on stimulating thirst, inhibits aldosterone secretion, inhibits renal absorption of Na+, inhibits renin release
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chance of male with CF having a child
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>5%, vas deferens is ****** up
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Women is pure vegan and breast feeds, baby gets what
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anemia from B12 deficiency
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EBV attaches to what on B cells
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CD21
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Hypogonadism and color blindness, lack of smell
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Kallman syndrome, absent GnRH
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hypogonadism, MR, retinitis pigmentosum
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Laurence-Moon-Biedl syndrome?
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turner's syndrome for boys
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Noonan syndrome
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male pseudohermaphrodite with cryptochoridism
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testicular femininization (absent androgen receptors, XR, most common cause of male pseudohermaphrodism)
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microdeletion syndrome with hypogonadism, mental retardation, short stature, and obesity
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Prader Willi( chromosome 15 paternal)
angelman is maternal |
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patient with neurofibromatosis has severe diastolic hypertension:
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probably pheochromocytoma
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Side effects of cyclophosphamide
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hemorrhagic cystitis and transitional carcinoma of the bladder ( remember also aniline dye)
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