Galactose, Fructose metabolism disorders Flashcards

1
Q

Deficiency in fructokinase

A

Essential fructosuria

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2
Q

Deficiency in aldose B

A

Fructose Intolerance

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3
Q

Deficiency in galactokinase

A

Galactokinase deficiency

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4
Q

Deficiency in galactose-1-phosphate uridyltransferase

A

Classical galactosemia

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5
Q

benign, asymptomatic condition

Facts appears in blood and urine

A

Essential fructosuria

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6
Q

Deficiency decreased the amount of available phosphte and results in the inhibition of glycogenolysis and gluconeogenesis

Symptoms present following consumption of fruit, juice, or honey.

Symptoms: hypoglycemia, jaudnice, cirrhosis, hepatomegaly, vomiting

A

Fructose intolerance

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7
Q

Accumulation of Galactitol.

Symptoms: galactose appears in blood and urine, infantile cataracts. May present as failure to track objects or to develop social smile

A

Galactokinase deficiency

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8
Q

Accumulation of galactitol (especially in the eye)

symptoms: failure to thrive, guidance, hepatomegaly, infantile cataracts, intellectual disability.

Can lead to E. coli sepsis in neonates

A

Classic galactosemia

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9
Q

What type of inheritance pattern does both galactose and fructose metabolism disorders have?

A

Autosomal recessive

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10
Q

Essential fructosuria

enzyme?
Symptoms?
and the reason why – symptoms?

A

Fructokinase

Benign, asymptomatic, fructose in blood and in urine

The reason it is benign is because hexokinase can convert fructose load (via diet) into Fructose-6-phosphate and that will enter glycolysis

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11
Q

Fructose intolerance

enzyme?
Symptoms?
Tx?

A

Aldose B

Traps phosphates
Symptoms appear after consumption of sugars (juice, fruit, honey)

hypoglycemia, jaundice, cirrhosis, vomiting, hepatomegaly

Tx: decrease intake of both fructose and sucrose (glucose + Fructose)

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12
Q

Galactokinase deficiency

enzyme?
Symptoms?

A

Galactokinase

Symptoms: galactose appears in blood and urine, infantile cataracts. May present as failure to track objects or to develop social smile

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13
Q

Classic galactosemia

enzyme?
Symptoms?
treatment?

A

galactose-1-phosphate uridyltransferase

symptoms: failure to thrive, guidance, hepatomegaly, infantile cataracts, intellectual disability.

Can lead to E. coli sepsis in neonates

Tx. exclude galactose and lactose (galactose + glucose) from diet

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