CYSTINE QUANTITATIVE, URINE (O.S.)

Requirements

Sample Required URINE
Preperations Required Clinical history, metabolic disorders or inborn errors of metabolism suspicion or provisional diagnosis of clincian required. Amino acid supplementation or medications need to stoped based on physician recommendations
Gender Male & Female
Age Group 0 - 70000 Years
Collection AtHome & Lab

₹ 7700

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CYSTINE QUANTITATIVE, URINE (O.S.)

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Overview

Cystinuria is an inborn error of metabolism(autosomal recessive disease) resulting from poor absorption and reabsorption of the amino acid cystine in the intestines and kidneys. This results in the production of kidney stones (urolithiasis)