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Phenylketonuria

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Phenylketonuria
Pathology
Type

Genetic

Cause(s)

Missing enzyme to process certain amino acids

Symptoms

Underdeveloped head, progressive impairment of cerebral function, hyperactivity, EEG abnormalities, seizures, learning disabilities

Mortality Rate

Moderate

Treatments

Control of diet, medication.

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Phenylketonuria at Wikipedia

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