clinical correlations Flashcards

(32 cards)

1
Q

Steatorrhea is ?

A

lipid malabsorption

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

In what disease process would you see increased lipids, essential fatty acids, and vitamins A D E K in feces

A

Steatorrhea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Treatment of Steatorrhea would be>

A

supplementation of short less than 6 carbon and medium 6-12 chain fatty acids

those type of FA don’t require micelle formation to absorb

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

NASH is

A

non alcoholic Steatorrhea hepatitis

fat build up killing liver

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Ketoacidosis results when ?

A

the rate of formation of ketone bodies is higher than the rate of use

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Ketoacidosis occurs in DM type 1 because excessive formation of ketone bodies forces___ ___ into ketone body pathway.

A

acetyl CoA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

In ketoacidosis the ketone body has a low pH causing what?

A

loses hydrogen to plasma, lowers physiological PH, results in metabolic acidosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Dehydration results from ketoacidosis because

A

excretion of excretion of glucose and ketone bodies in the urine.
water follows the ketone bodies and sugar

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Mom with a premature baby. Give what before delivery to do what?

surfactant

A

glucocorticoids to speed lung maturation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Toxins, venoms, and pathogenic bacteria have______activity and may dissolve_____ and spread______

A

phospholipase
membranes
infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

An accumulation of glycosphingolipids would result from a

A

genetic issue such as tay-sachs from deficient enzymes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
  • accumulation of gangliosides
  • rapid progressive fatal neurodegeneration
  • blindness
  • cherry red macula
  • muscular weakness
  • seizures
A

tay -sachs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

a neurotoxic medical emergency that would have the S/S of tremors, slurred speech, somnolence, blurred vision, coma, death would be caused by

6

A

hyperammonemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what would the cause of hyperammonemia be?

A

ammonia formation exceeds urea cycle capacity due to declining liver function related to hepatic disease that results in deficient urea cycle enzymes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

high homocysteine levels from methionine metabolism would result in

A

neural tube defect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

elevated homocysteine levels from methionine metabolism is related to atherosclerosis why?

A

foam cells

elevated homocysteine promotes oxidative damage, inflammation, and endothelial damage

17
Q

what supplement would you give to lower homocysteine?

18
Q

PKU (phenylketonuria) causes what and newborns

A

mental retardation

19
Q

How do you treat PKU?

A

foods low in phenylalanine

give tyrosine

20
Q

What’s the biochemical problem with PKU

A

don’t have the enzymes to covert phenylalanine to tyrosine, phenylpyruvate(toxic) builds up

21
Q

name the issue caused by a defect in tyrosine metabolism

A

albinism-deficiency in melanin

22
Q

name the catecholamines derived from tyrosine

4

A
tyrosine 
dopa
dopamine 
norepi 
epi
23
Q

histamine is formed from ______by what process?

A

histidine

decarboxylation

24
Q

Serotonin is made from

25
serotonin is a NT that causes _____,______ and ______.
vasoconstriction smooth muscle contraction platelet aggregation
26
GABA is produced from glutamate by ?
glutamate decarboxylase
27
Arginine is synthesized to ____by being catalyzed by NO synthase.
NO | NO synthase
28
an autosomal recessive disease that causes mutation of Chloride channel
cystic fibrosis
29
In cystic fibrosis chloride conductance is ______
decreased
30
In cystic fibrosis decreased chloride conductance causes an increase in?
sodium and water retention
31
S/S of cystic fibrosis
increased thickening secretions and pancreatic enzymes that don't reach intestine
32
Treat CF with
pancreatic enzymes