Endocrine disorders

Institution TVET
Course DIPLOMA IN NURSING
Year 1st Year
Semester Unknown
Posted By stephen oyake rabilo
File Type pdf
Pages 33 Pages
File Size 499.39 KB
Views 4262
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Description

It is an Autosomal recessive inborn error of metabolism found on the twelfth chromosome Causing an inherited metabolic disease that passes through families. It is rare condition characterized by the deficiency in the enzyme (Phenylalanine Hydroxylase). Normally: phenylalanine tyrosine by liver enzyme phenylalanine hydroxylase (PAH)
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