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LIVER FUNCTION TEST part 4

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

uses Diazotized sulfanilic acid for Bilirubin used in serum

Back (Answer)

Van Den Berg Reaction

#2
Front (Question)

Van Den Berg Reaction uses this acid in serum.

Back (Answer)

Diazotized sulfanilic acid

#3
Front (Question)

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

Back (Answer)

sodium nitrate and hydrochloric acid

#4
Front (Question)

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

Back (Answer)

Icterus Index

#5
Front (Question)

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

Back (Answer)

saline 0.01% potassium dichromate solution

#6
Front (Question)

What are the interferences in Icterus Index?

Back (Answer)

 Carotene  Xanthophyll  Hemoglobin

#7
Front (Question)

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

Back (Answer)

455nm

#8
Front (Question)

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

Back (Answer)

575nm

#9
Front (Question)

Problem causing jaundice occurs before liver metabolism

Back (Answer)

Pre-hepatic Jaundice

#10
Front (Question)

What caused the pre-hepatic Jaundice?

Back (Answer)

Increased amount of bilirubin being presented in the liver

#11
Front (Question)

Unconjugated hyperbilirubinemia

Back (Answer)

PRE-HEPATIC JAUNDICE

#12
Front (Question)

Intrinsic liver disease

Back (Answer)

HEPATIC JAUNDICE

#13
Front (Question)

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

Back (Answer)

UGT1A1

#14
Front (Question)

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

Back (Answer)

Gilbert’s Syndrome

#15
Front (Question)

 has a defective hepatic uptake of bilirubin

Back (Answer)

Gilbert’s Syndrome

#16
Front (Question)

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

Back (Answer)

Crigler-Najjar Syndrome

#17
Front (Question)

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

Back (Answer)

Crigler-Najjar Syndrome

#18
Front (Question)

 total UDPGT deficiency  complete absence of enzymatic bilirubin conjugation

Back (Answer)

Type I Crigler-Najjar Syndrome

#19
Front (Question)

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

Back (Answer)

Type II Crigler-Najjar Syndrome

#20
Front (Question)

defective hepatic excretion of bilirubin

Back (Answer)

Dubin-Johnson Syndrome

#21
Front (Question)

What caused the Dubin-Johnson Syndrome?

Back (Answer)

deficiency of the canalicular transporter protein (MDR2/CMOAT)

#22
Front (Question)

defective hepatic excretion of bilirubin; has normal gall bladder function

Back (Answer)

Rotor Syndrome

#23
Front (Question)

What causes the Rotor Syndrome?

Back (Answer)

reduction in the concentration or activity of intracellular binding proteins.

#24
Front (Question)

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

Back (Answer)

TRUE