Endocrine disorders
| Institution | TVET |
| Course | DIPLOMA IN NURSING |
| Year | 1st Year |
| Semester | Unknown |
| Posted By | stephen oyake rabilo |
| File Type | |
| Pages | 33 Pages |
| File Size | 499.39 KB |
| Views | 8623 |
| Downloads | 0 |
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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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