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SGCD Gene Limb-girdle muscular dystrophy, autosomal recessice type 2F NGS Genetic Test

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SGCD Gene Limb-girdle muscular dystrophy, autosomal recessice type 2F NGS Genetic Test

Short Name: SGCD Gene LGMD 2F NGS Test

Also known as: Autosomal recessive limb-girdle muscular dystrophy 2F, LGMD2F

SGCD Gene Limb-girdle muscular dystrophy, autosomal recessice type 2F NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS (Next-Generation Sequencing) 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

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

The purpose of this test is to identify mutations in the SGCD gene that cause autosomal recessive limb-girdle muscular dystrophy type 2F, enabling accurate diagnosis, genetic counseling, and informed management decisions.

Test Code
1664
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 (Next-Generation Sequencing)
Step 1

Sample Collection

Provide clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of affected family members.

Step 2

Laboratory Analysis

Blood sample collection via venipuncture or use of FTA card for one drop of blood.

Step 3

Report Delivery

Sample is labeled and sent to the laboratory for NGS analysis.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling session and review of clinical history.
2
During the Test:Blood sample collection for DNA extraction and NGS analysis.
3
After the Test:Laboratory analysis, report generation, and genetic counseling if needed.

About This Test

Who Should Get This Test

The purpose of this test is to identify mutations in the SGCD gene that cause autosomal recessive limb-girdle muscular dystrophy type 2F, enabling accurate diagnosis, genetic counseling, and informed management decisions.

How to Prepare

  • No special preparation required
  • Ensure sample is properly labeled
  • Home collection available with prior booking

Doctor's Notes

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

"Early diagnosis through NGS genetic testing is vital for managing symptoms and preventing complications in hereditary neuromuscular disorders like LGMD2F."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Blood sample stable at room temperature for up to 48 hours
Extracted DNA stable at -20°C for long-term storage
Sample Rejection Criteria:
  • Clotted or hemolyzed sample
  • Insufficient sample volume
  • Unlabeled or mislabeled sample

Understanding Your Results

Results should be interpreted by a qualified geneticist or physician in the context of clinical findings and family history.
📊

No pathogenic variant detected

SGCD gene mutation not identified. Consider other genetic causes or further clinical evaluation.

📊

Pathogenic variant detected

Confirms diagnosis of SGCD-related limb-girdle muscular dystrophy type 2F. Genetic counseling recommended for the family.

⚠️ When to Consult a Doctor:

Consult a neurologist or geneticist if there are symptoms of progressive muscle weakness, difficulty in movement, or a family history of muscular dystrophy.

Limitations

  • ⚠Test may not detect all possible genetic variations
  • ⚠Results require clinical correlation with symptoms and family history
  • ⚠Genetic counseling is recommended for interpretation

Risks & Considerations

  • ●Minor bruising at the puncture site
  • ●Rare risk of infection
  • ●Possible discomfort during blood draw

Interfering Factors

  • ●Hemolyzed blood sample
  • ●Sample contamination
  • ●Improper storage of sample

Compare With Similar Tests

TestSGCD Gene Limb-girdle muscular dystrophy, autosomal recessice type 2F NGS Genetic TestDMD Gene NGS Genetic TestDYSF Gene NGS Genetic Test
ComparisonSGCD Gene Limb-girdle muscular dystrophy, autosomal recessice type 2F NGS Genetic Test

Frequently Asked Questions

What is the SGCD Gene Limb-girdle Muscular Dystrophy NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the SGCD gene, causing autosomal recessive limb-girdle muscular dystrophy type 2F.
How much does the SGCD Gene LGMD 2F NGS Genetic Test cost?
The test costs INR 20000 in India, with free home sample collection available.
What samples are required for this genetic test?
Samples can be blood, extracted DNA, or one drop of blood on an FTA card.
Is home collection available for this test?
Yes, free home sample collection is offered for online bookings across many cities in India.
How long does it take to receive results?
Results are typically available within 3 to 4 weeks after sample collection.
Is this test covered by insurance or government schemes?
Coverage varies; check with your insurance provider or government schemes like PMJAY or CGHS.
What symptoms indicate the need for this genetic test?
Symptoms include progressive muscle weakness in hips and shoulders, difficulty climbing stairs, waddling gait, and family history of muscular dystrophy.
Who should undergo this genetic test?
Individuals with symptoms of limb-girdle muscular dystrophy, family history of the condition, or elevated muscle enzyme levels should consider testing.
What is the accuracy of NGS genetic testing for LGMD2F?
NGS is highly accurate for detecting SGCD gene mutations, but results should be correlated with clinical findings.
Can children be tested for this condition?
Yes, the test can be performed on individuals of all ages, including children, especially if symptoms are present.
What should I do if the test results are positive?
A positive result confirms LGMD2F; consult a geneticist for counseling, management options, and family planning advice.
Are there any risks associated with the test?
Risks are minimal, such as minor bruising at the blood draw site or rare infection risk.
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.

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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.

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✓ 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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