LIVER FUNCTION TEST part 4 Flashcards

(30 cards)

1
Q

uses Diazotized sulfanilic acid for Bilirubin used in serum

A

Van Den Berg Reaction

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2
Q

Van Den Berg Reaction uses this acid in serum.

A

Diazotized sulfanilic acid

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3
Q

the diazotized sulfanilic acid is formed by reacting sulfanilic acid with _________________

A

sodium nitrate and hydrochloric acid

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4
Q

This is often subjective and the test involves diluting serum with saline until it visually
matches the color of a 0.01% potassium dichromate solution

A

Icterus Index

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5
Q

Icterus Index test involves diluting serum with __________ until it visually matches the color of a ____________________

A

saline
0.01% potassium dichromate solution

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6
Q

What are the interferences in Icterus Index?

A

 Carotene
 Xanthophyll
 Hemoglobin

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7
Q

In DIRECT SPECTROPHOTOMETRIC METHOD, what is the wavelength at which bilirubin in serum is measured?

A

455nm

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8
Q

the absorbance of hemoglobin is 455 nm which can be corrected by subtracting the absorbance at ____________

A

575nm

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9
Q

Problem causing jaundice occurs before liver metabolism

A

Pre-hepatic Jaundice

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10
Q

What caused the pre-hepatic Jaundice?

A

Increased amount of bilirubin being presented in the liver

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11
Q

Unconjugated hyperbilirubinemia

A

PRE-HEPATIC JAUNDICE

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12
Q

Intrinsic liver disease

A

HEPATIC JAUNDICE

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13
Q

In Gilbert’s Syndrome, this is reduced in the expression of gene.

A

UGT1A1

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14
Q

 intermittent hyperbilirubinemia
 inherited bilirubin derangement
 Reduced conjugating capability of the liver

A

Gilbert’s Syndrome

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15
Q

 has a defective hepatic uptake of bilirubin

A

Gilbert’s Syndrome

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16
Q

has a defective conjugation of bilirubin due to the deficiency of the enzyme UDPGT

A

Crigler-Najjar Syndrome

17
Q
  • Chronic unconjugated hyperbilirubinemia
  • Molecular defect w/in the gene involved with bilirubin conjugation
  • Rare & more serious disorde
A

Crigler-Najjar Syndrome

18
Q

 total UDPGT deficiency
 complete absence of enzymatic bilirubin conjugation

A

Type I Crigler-Najjar Syndrome

19
Q

 partial UDPGT deficiency
 the mutation causing a severe deficiency of the enzyme for Conjugation

A

Type II Crigler-Najjar Syndrome

20
Q

defective hepatic excretion of bilirubin

A

Dubin-Johnson Syndrome

21
Q

What caused the Dubin-Johnson Syndrome?

A

deficiency of the canalicular transporter protein (MDR2/CMOAT)

22
Q

defective hepatic excretion of bilirubin; has normal gall bladder function

A

Rotor Syndrome

23
Q

What causes the Rotor Syndrome?

A

reduction in the concentration or activity of intracellular binding proteins.

24
Q

TRUE OR FALSE:
Liver biopsy does NOT show dark pigmented granules

25
it has a presence of circulating antibody against UDPGT
Lucey-Driscoll Syndrome
26
 deposition of bilirubin in the nuclei of brain & nerve  cells-cell damage & death of newborn
Kernicterus
27
 Usually results from biliary obstructive disease (e.g. gallstones, tumors)  Prevents the flow of conjugated bilirubin into the bile canaliculi  Clay-colored stool
POST-HEPATIC JAUNDICE
28
What happens when bilirubin is exposed to light?
Photo-oxidize
29
conjugated bilirubin that is covalently bound to albumin
Delta Bilirubin
30
the ______________ enhances or accelerates the unconjugated bilirubin reaction with diazotized sulfanilic acid
accelerator agents