Inborn Errors of Metabolism

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What of the following is true about the one-gene one-enzyme hypothesis
Each gene codes for a specific enzyme
1 of 6
What is the metabolic deficiency of Phenylketonuria?
Phenylalanin is not metabolised to tyrosine
2 of 6
What is one of the main symptoms of phenylketonuria?
Musty odour in breath, skin and urine
3 of 6
The lack of oxidation of which acid leads to Alkaptonuria?
Homogentisic acid
4 of 6
What is a symptom of Alkaptonuria?
Arthritis in the knees and hips
5 of 6
What is another name for MSUD
Branched-chain keto aciduria
6 of 6

Other cards in this set

Card 2

Front

What is the metabolic deficiency of Phenylketonuria?

Back

Phenylalanin is not metabolised to tyrosine

Card 3

Front

What is one of the main symptoms of phenylketonuria?

Back

Preview of the front of card 3

Card 4

Front

The lack of oxidation of which acid leads to Alkaptonuria?

Back

Preview of the front of card 4

Card 5

Front

What is a symptom of Alkaptonuria?

Back

Preview of the front of card 5
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