CYSTINE QUANTITATIVE, URINE (O.S.)

Requirements

  • Sample Analyzing Icon

    Sample Required Urine

  • Sample Analyzing Icon

    Preperations Required Clinical history, suspicion of metabolic diseases or inborn errors of metabolism, fasting recommendation but not requirement, and preliminary diagnosis of the clinician are all necessary. According to doctor's advice, amino acid supplements or drugs need

  • Sample Analyzing Icon

    Gender Male & Female

  • Sample Analyzing Icon

    Age Group 0 - 99 Years

  • Sample Analyzing Icon

    Collection AtHome & Lab

7700
Add to Cart arrow-icon
  • Sample Analyzing Icon

    1 Observations included

  • Sample Analyzing Icon

    Results with in 10 Days

10% off New user? Enjoy 10% off up to Rs 200 on all tests and health packages.

Use Code: NEW10

CYSTINE QUANTITATIVE, URINE (O.S.)

Observations Included

Sample Analyzing Icon

10,000+ Tests Done

Sample Analyzing Icon

Trusted By Doctors

Sample Analyzing Icon

NABL Certified Labs

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), which can cause severe pain and potential urinary tract obstruction.

whatsapp-icon Need Help