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Phenylketonuria
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Published on Jan 21, 2016
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PRESENTATION OUTLINE
1.
PHENYLKETONURIA
2.
WHAT IS IT
When a baby is born without the ability to break down amino acids
3.
SYMPTOMS
infants with the condition often have lighter skin, hair, and eyes than brothers or sisters without the disease.
Delayed mental and social skills
Head size significantly below normal
Jerking movements of the arms or legs
intellectual disability
4.
TREATMENT
A diet that is very low in phenylalanine
A special infant formula called Lofenalac
Fish oil supplements
5.
PROGNOSIS
If the diet is started right after birth then the kid should be fine
But if the treatment is delayed or not treated then brain damage will happen
If proteins containing phenylalanine are not avoided, PKU can lead to intellectual disability by the end
^of the first year of life.
ADHD is possible
6.
MUTATION
Autosomal recessive
7.
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