Skip to main content
DNA Labs India

Amino Acids Qualitative CSF Test

DNA Labs India | ISO 9001:2015 Certified

Amino Acids Qualitative CSF Test

Short Name: Amino Acids CSF Test

Also known as: CSF Amino Acid Test, Qualitative Amino Acids in CSF

Amino Acids Qualitative CSF Test test available at DNA Labs India for ₹1,404. Uses Thin Layer Chromatography, One dimensional on Cerebrospinal Fluid (CSF) samples. Results in Results typically available within 2 days after sample receipt.. Free home collection in 300+ cities across India.

PediatricianPediatric🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Amino Acids Qualitative CSF Test is to diagnose and monitor conditions related to abnormal amino acid metabolism, aiding in the early detection of inborn errors of metabolism such as Phenylketonuria (PKU) and Maple Syrup Urine Disease (MSUD).

Test Code
99
Price
₹1,404
Sample Type
Cerebrospinal Fluid (CSF)
Result Time
Results typically available within 2 days after sample receipt.
Fasting Required
No
Method
Thin Layer Chromatography, One dimensional
Step 1

Sample Collection

Provide clinical details and drug history. No specific fasting required, but ensure all necessary information is documented.

Method: Lumbar puncture

Step 2

Laboratory Analysis

CSF collected via lumbar puncture by a trained healthcare professional in a sterile environment.

Step 3

Report Delivery

Sample must be shipped refrigerated or frozen to the laboratory for analysis.

Timeline: Results typically available within 2 days after sample receipt.

Patient Instructions

1
Before the Test:Provide clinical details and drug history. No fasting required, but ensure all patient information is available.
2
During the Test:CSF sample collected via lumbar puncture; procedure typically takes 30-60 minutes.
3
After the Test:Sample sent to lab for analysis; results available in 2 days.

About This Test

Who Should Get This Test

The purpose of the Amino Acids Qualitative CSF Test is to diagnose and monitor conditions related to abnormal amino acid metabolism, aiding in the early detection of inborn errors of metabolism such as Phenylketonuria (PKU) and Maple Syrup Urine Disease (MSUD).

How to Prepare

  • Collect 1 mL (minimum 0.5 mL) of CSF in a sterile screw capped vial.
  • Ship refrigerated or frozen to maintain sample integrity.
  • Include clinical details and drug history with the sample.

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Early detection through CSF amino acid analysis can significantly improve outcomes in metabolic disorders, especially in children with unexplained neurological symptoms."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeCerebrospinal Fluid (CSF)
Sample Volume1 mL (0.5 mL min.)
ContainerSterile screw capped vial
Collection MethodLumbar puncture

Sample Stability

Room Temperature: Not applicable (NA)
Refrigerator: 48 hours
Frozen: 2 weeks
Sample Rejection Criteria:
  • Insufficient sample volume (<0.5 mL)
  • Improper container or contaminated sample
  • Missing clinical details or drug history
  • Sample not shipped refrigerated or frozen as required

Understanding Your Results

Results indicate whether the amino acid profile in CSF is normal or abnormal, suggesting potential inborn errors of metabolism.
Normal amino acid pattern: No evidence of metabolic disorders based on qualitative analysis.
Abnormal amino acid pattern: Suggests possible inborn error of metabolism; correlation with clinical symptoms and further testing is essential.
Abnormal results may require follow-up with quantitative tests, genetic analysis, or enzyme assays for confirmation.
⚠️ When to Consult a Doctor:

If the test shows abnormal results or if symptoms such as developmental delays, seizures, or behavioral problems persist, consult a healthcare provider or specialist for further evaluation and management.

Limitations

  • Qualitative analysis only; does not quantify amino acid levels
  • May require confirmatory tests like plasma amino acid analysis or genetic testing
  • Results must be interpreted in clinical context with other diagnostic findings

Risks & Considerations

  • Headache after lumbar puncture
  • Risk of infection at puncture site
  • Minor bleeding or discomfort
  • Rarely, nerve damage or CSF leak

Interfering Factors

  • Drug history (must accompany sample)
  • Recent lumbar puncture or spinal procedures
  • Contamination of CSF sample during collection

Compare With Similar Tests

TestAmino Acids Qualitative CSF TestPlasma Amino Acid AnalysisUrine Organic Acid AnalysisGenetic Testing
ComparisonAmino Acids Qualitative CSF TestQuantitative analysis of amino acids in blood; may be used alongside CSF test for comprehensive assessment.Detects organic acids in urine; complementary for diagnosing metabolic disorders.Identifies specific genetic mutations; often confirmatory for inborn errors of metabolism.

Frequently Asked Questions

What is the Amino Acids Qualitative CSF Test?
It is a diagnostic test that analyzes cerebrospinal fluid to detect abnormal amino acid levels, helping identify inborn errors of metabolism.
Why is this test performed?
To diagnose and monitor conditions like Phenylketonuria (PKU), Maple Syrup Urine Disease (MSUD), and other metabolic disorders indicated by symptoms such as developmental delays or seizures.
How is the sample collected?
A CSF sample is collected via lumbar puncture by a healthcare professional and shipped refrigerated or frozen to the lab.
What is the cost of the test?
The test costs INR 1404 at DNA Labs India, with free home sample collection available in many cities across India.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities.
What is the turnaround time for results?
Results are typically available within 2 days after sample receipt.
Are there any risks associated with CSF collection?
Risks include headache, infection, or bleeding at the puncture site, but these are generally rare when performed by skilled professionals.
What conditions can this test detect?
It can detect conditions such as Phenylketonuria (PKU), Maple Syrup Urine Disease (MSUD), Tyrosinemia, Citrullinemia, and Homocystinuria.
How should I prepare for the test?
No special preparation is needed, but ensure clinical details and drug history are provided to accompany the sample.
What do abnormal results mean?
Abnormal results suggest possible inborn errors of metabolism; consult a healthcare provider for further evaluation and confirmatory testing.
Is fasting required for this test?
No, fasting is not required, but accurate clinical information must be provided.
How can I book the test?
You can book the test online through DNA Labs India's website or contact their customer service for assistance.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

Related Tests

For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.