Skip to main content
DNA Labs India

FLNB Gene Spondylocarpotarsal synostosis syndrome NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

FLNB Gene Spondylocarpotarsal synostosis syndrome NGS Genetic Test

FLNB Gene Spondylocarpotarsal synostosis syndrome 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 identify mutations in the FLNB gene for accurate diagnosis of Spondylocarpotarsal synostosis syndrome, aiding in clinical management and genetic counseling.

Test Code
2481
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 Spondylocarpotarsal synostosis syndrome.

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:Clinical history review and genetic counseling session.

About This Test

Who Should Get This Test

To identify mutations in the FLNB gene for accurate diagnosis of Spondylocarpotarsal synostosis syndrome, aiding in clinical management and genetic counseling.

How to Prepare

  • Blood sample collection via venipuncture
  • Alternatively, use extracted DNA or one drop of blood on FTA card

Doctor's Notes

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

"Early genetic testing for FLNB mutations can guide management and family planning for skeletal disorders."

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 pathogenic mutations in the FLNB gene. A positive result confirms diagnosis, while a negative result may require further clinical evaluation.
📊

Positive

Pathogenic variant detected, confirming Spondylocarpotarsal synostosis syndrome.

📊

Negative

No pathogenic variants detected; clinical correlation recommended.

⚠️ When to Consult a Doctor:

When experiencing symptoms such as fused bones, scoliosis, hip dysplasia, hearing loss, or stiffness, or with a family history of skeletal disorders.

Frequently Asked Questions

What is the FLNB Gene Spondylocarpotarsal synostosis syndrome NGS Genetic Test?
It is a next-generation sequencing test to detect mutations in the FLNB gene, which causes Spondylocarpotarsal synostosis syndrome, a rare skeletal disorder.
What are the symptoms of Spondylocarpotarsal synostosis syndrome?
Symptoms include fused vertebrae, fused bones in hands and feet, scoliosis, hip dysplasia, hearing loss, stiffness, and limited movement.
How is the test performed?
The test uses next-generation sequencing technology on a blood sample, extracted DNA, or blood on an FTA card.
What is the cost of the test?
The test costs INR 20,000 at DNA Labs India, with free home sample collection available.
Is fasting required for the test?
No, fasting is not required for this genetic test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks.
Who should consider this test?
Individuals with symptoms of skeletal disorders or a family history of Spondylocarpotarsal synostosis syndrome should consider testing.
What does a positive result mean?
A positive result indicates a pathogenic mutation in the FLNB gene, confirming the diagnosis.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test across India.
What is the sample type for the test?
The sample can be blood, extracted DNA, or one drop of blood on an FTA card.
Can the test be used for prenatal diagnosis?
Consult a healthcare professional for prenatal testing options, as this test is typically for postnatal diagnosis.
How accurate is the NGS genetic test?
NGS technology provides high accuracy in detecting mutations, but results should be interpreted by a qualified geneticist.
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.