exam 1 pt 3 Flashcards

1
Q

what is necroptosis?

A

cell murder that is programmed
and includes inflammatory changes

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2
Q

what is necrosis

A

-cell autodigestion. autolysis that happens in result of ischemia, chemical injury or secondarily hypoxia

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3
Q

three things that happen in necrosis?

A

unregulates enzyme digestion of cell components, loss of membrane integrity and inflammatory response

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4
Q

pyknosis, karynorrhexis and karyolysis is part of?

A

necrosis

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5
Q

what are 4 necrosis types?

A

liquifactive, coagulative, caseous and fat necrosis

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6
Q

liquifactive necrosis

A

cell digested by their own enzymes
-brain abcess

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7
Q

coagulative necrosis

A

-hypoxic injury where acidosis has happened that denatures enzymes and proteins of cells

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8
Q

what is infarct

A

the area of coagulative necrosis

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9
Q

where does coagulative necrosis happen?

A

kidney, hear and adrenal glands

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10
Q

pulmonary tb and mycobacterium tb cause?

A

caseous necrosis

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11
Q

tb granumola is?

A

caseous where the inflammatory wall closes off the necrosis area

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12
Q

what is caused by pancreatic lipases?

A

fat necrosis bc free fatty acid saponify with ca

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13
Q

where does fat necrosis happen

A

breast and pancreas

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14
Q

what type of gangrene swells?

A

wet gangrene due to the lack of venous flow

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15
Q

what type of gangrene affects ONLY extremeties?

A

dry gangrene

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16
Q

what gangrene is the result of coagulative necrosis?

A

dry gangrene
-slow spread and NO bacterial infection

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17
Q

what is secondary to necrotizing bacterial infection?

A

wet gangrene

18
Q

does wet gangrene have a line of demarcation?

A

no

19
Q

wet gangrene tissue?

A

pulseless, cols, swollen and black
-rapid spread
-internal organs

20
Q

missence

A

single aa changes

21
Q

frameshift

A

indel

22
Q

mrna forms?

A

template for protein synth in codons

23
Q

rrna is?

A

part of the ribosome and made in nucleus

24
Q

tRNA binds to?

A

specific aa to transfer to ribosome

25
Q

what is marfan syndrom?

A

autosomal dom
-connective tissue disorder affecting fibrillin 1
-parts of microfibrils are in ecm

26
Q

ar with one copy

A

is a carrier but phenotypically normal
-only in one generation

27
Q

taysachs, pku, cf and sickle cell are?

A

ar

28
Q

lysosomal storage disease

A

tay sachs

29
Q

mental retardation, microcephaly, seizure, delay speeck, bad breath, hypopigmentation and high toxic metabolites are symptoms of?

A

pku

30
Q

low protein diet for?

A

pku

31
Q

affected male give carrier gene to daughters if?

A

x link recessive
-all sons normal bc they only get y

32
Q

xr daughters have what genotype?

A

carriers that are phenotypically normal but can have affected sons

33
Q

xd affects?

A

both male and female and has no generational skips
-50% of the f1’s offspring is affected regardless of sex
-no male to male transmission inly 50% daughters affected

34
Q

fragile x syndrome is?

A

xd

35
Q

deletion, translocation, inversion and robertsonian affect?

A

chromosomes

36
Q

monosomy

A

one chromosome copy

37
Q

polysomy

A

more than 2 copies

38
Q

trisonomy 21 manifestations

A

intellectual disable, flat facies, epicanthal fold, low malform ears, open mouth and macroglossia, short hands, 1 and 2 toe gap

39
Q

when do you screen for 21?

A

btwn trimester 1 and 2

40
Q

what is elevated in downs?

A

human chrionic gonadotropin and inhibin A

41
Q

what is low in dows?

A

estriol and alpha fetoprotein

42
Q

what is seen on downs ultrasound?

A

nuchal translucency