G6PD Flashcards

1
Q

Definition of G6PD?
What kind of disease?
What does it cause?

A

X linked recessive (mostly men) enzymopathy
Due to decreased glucose-6-phosphate dehydrogenase =destruction of RBC

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2
Q

How is defective G6PD enzymes different to normal enzymes?

A

Shorter half life - doesn’t last as long

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3
Q

Symptoms of G6PD

A

Mostly asymptomatic unless precipitated/triggered
(Due to high free radicals production)

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4
Q

Causes of G6PD that trigger symptoms

A

Food & drinks = fava beans, soy products & red wine
Anti malarials = quinine
Meds = aspirin, ibuprofen
Nitrofurantoin + trimethoprim

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5
Q

What type of haemolysis do RBCs undergo in G6PD anemia?

A

Intravascular

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6
Q

When an attack is taking place, what symptoms occur? G6PD

A

Rapid anemia + Jaundice

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7
Q

What causes G6PD jaundice to occur?
Pathology

A

Hb = Globin + Heme
Heme —> bilirubin—> taken up by liver cells —> secreted in bile (normally)

Haemolysis = excess bilirubin
—> stay in blood = jaundice (bilirubin deposits in skin/eyes)
—> urobilin = urine (tea like colour)

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8
Q

G6PD Diagnosis?
Tests?

A

FBC + blood film
Normal in between attacks

Attack = normocytic normochromic with high reticulocytes
Heinz bodies + bite cells

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9
Q

Why do you see Heinz bodies in G6PD?

A

Free radicals directly damage Hb (carry O2) , these proteins precipitate inside RBC

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10
Q

Why do we see bite cells in G6PD?

A

Splenic macrophages try remove them by eating them

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11
Q

Treatment of G6PD?

A

Avoid precipitants/triggers
Blood transfusion when attack occurs

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12
Q

Where is G6PD disease most common and why is it good for that particular region?

A

Africa + Asia
Protect against malaria

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