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	4089
Downloads	0
Price:	Ksh. 50 Buy Now Buy via whatsapp

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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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