Phenylketonuria.. Phenylalanine hydroxylase deficiency is necessary to convert phenylalanine into tyrosine. Sclerosis in the thighs and buttocks

Phenylketonuria:
This disease affects children with blond hair, blue eyes and light skin due to the deficiency of phenylalanine hydroxylase necessary to convert phenylalanine into tyrosine.
Clinical manifestations:
- Photodynamic sensitivity.
- Triggering of eczema (pseudo-eczema).
Secondary infections (common).
- Skin lesions similar to scleroderma.
- Stenosis in the thighs and buttocks are common manifestations in infants and infected children.
General features:
- Retardation.
Epileptic seizures.
Laboratory assets:
- The presence of vinyl peruvic acid in the urine and this can be easily determined by adding a few drops of iron chlorine solution to the urine (veric chloride) and this may give a dark green color.
Treatment methods:
- Special diet for infants and young children Container on a little phenyl whining should be given immediately after birth.
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