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 | 8599 |
| Downloads | 0 |
| Price: |
Buy Now
 Buy via
whatsapp
|
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)
Below is the document preview.
KCSE FORM 1 CHEMISTRY NOTES
Trending!
UPDATED KCSE FORM1 CHEMISTRY NOTES
117 Pages
8658 Views
1 Downloads
2.43 MB
KCSE FORM 2 CHEMISTRY NOTES
Trending!
UPDATED KCSE FORM2 CHEMISTRY NOTES
137 Pages
5155 Views
0 Downloads
1.73 MB
KCSE FORM 3 CHEMISTRY NOTES
Trending!
UPDATED KCSE FORM3 CHEMISTRY NOTES
262 Pages
6421 Views
2 Downloads
2.11 MB
KCSE FORM 4 CHEMISTRY NOTES
Trending!
UPDATED KCSE FORM4 CHEMISTRY NOTES
334 Pages
4988 Views
2 Downloads
4.44 MB