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DNA Labs India

BSND Gene Bartter syndrome type 4a NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

BSND Gene Bartter syndrome type 4a NGS Genetic Test

Short Name: BSND Gene Test

Also known as: Bartter Syndrome Type 4a, BSND-related Bartter syndrome

BSND Gene Bartter syndrome type 4a NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Bartter Syndrome Type 4a by detecting mutations in the BSND gene using Next-Generation Sequencing (NGS) technology.

Test Code
2561
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Bartter Syndrome Type 4a.

Step 2

Laboratory Analysis

Your sample is analyzed using NGS Technology in our laboratory.

Step 3

Report Delivery

A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review are recommended before testing.
2
During the Test:Sample collection via blood draw or DNA extraction.
3
After the Test:Results are available in 3 to 4 weeks; follow-up with a genetic specialist is advised.

About This Test

Who Should Get This Test

To diagnose Bartter Syndrome Type 4a by detecting mutations in the BSND gene using Next-Generation Sequencing (NGS) technology.

How to Prepare

  • Provide blood sample or extracted DNA
  • Use FTA card for one drop blood if applicable

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card

Understanding Your Results

Results indicate the presence or absence of mutations in the BSND gene associated with Bartter Syndrome Type 4a.
📊

Mutation detected

Confirms diagnosis of Bartter Syndrome Type 4a; genetic counseling recommended.

📊

No mutation detected

Bartter Syndrome Type 4a unlikely; consider other causes if symptoms persist.

⚠️ When to Consult a Doctor:

If you experience symptoms such as muscle weakness, fatigue, heart palpitations, low blood pressure, increased thirst and urination, or growth delay in children, consult a healthcare provider for evaluation.

Risks & Considerations

  • Minimal physical risks from blood draw
  • Potential psychological impact of genetic results

Frequently Asked Questions

What is Bartter Syndrome Type 4a?
Bartter Syndrome Type 4a is a rare genetic disorder affecting the kidneys, causing electrolyte imbalances due to mutations in the BSND gene.
What causes Bartter Syndrome Type 4a?
It is caused by mutations in the BSND gene, which impairs kidney function and electrolyte reabsorption.
What are the symptoms of Bartter Syndrome Type 4a?
Symptoms include muscle weakness, fatigue, heart palpitations, low blood pressure, increased thirst and urination, and growth delay in children.
How is Bartter Syndrome Type 4a diagnosed?
Diagnosis is typically through genetic testing to detect BSND gene mutations, along with blood and urine tests for electrolyte imbalances.
What is the BSND Gene NGS Genetic Test?
It is a Next-Generation Sequencing test that analyzes the BSND gene for mutations to confirm Bartter Syndrome Type 4a.
What is the cost of the BSND Gene Test in India?
The cost is approximately INR 20,000, with home sample collection available across India.
Is the test covered by insurance?
It is typically covered by insurance, but coverage should be confirmed with your provider.
How is the sample collected for the test?
Sample can be collected via blood, extracted DNA, or one drop blood on an FTA card, with home collection available.
What is the turnaround time for results?
Results are typically available in 3 to 4 weeks.
Are there any risks associated with the test?
Risks are minimal, mainly related to blood draw, with potential psychological impact from results.
How can I prepare for the test?
Provide clinical history and undergo genetic counseling to draw a family pedigree chart.
What should I do if I test positive?
Consult a genetic specialist or nephrologist for management and genetic counseling.
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.
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.

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