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LBR Gene Greenberg skeletal dysplasia NGS Genetic Test

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LBR Gene Greenberg skeletal dysplasia NGS Genetic Test

LBR Gene Greenberg skeletal dysplasia NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3-4 weeks. Free home collection in 300+ cities across India.

PediatricsPediatric🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect mutations in the LBR gene associated with Greenberg skeletal dysplasia for accurate diagnosis and genetic counseling.

Test Code
2741
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3-4 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with LBR gene-related conditions.

Step 2

Laboratory Analysis

Your sample is analyzed using Next-Generation Sequencing (NGS) 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: 3-4 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 saliva collection.
3
After the Test:Results are delivered in 3-4 weeks; follow-up with a healthcare provider is advised.

About This Test

Who Should Get This Test

To detect mutations in the LBR gene associated with Greenberg skeletal dysplasia for accurate diagnosis and genetic counseling.

How to Prepare

  • For blood sample: Standard venipuncture procedure.
  • For saliva sample: Use provided collection kit.
  • For FTA card: Collect one drop of blood.

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 LBR gene. Consult a genetic counselor or healthcare professional for interpretation.
📊

Positive

Pathogenic variant detected in LBR gene, indicating Greenberg skeletal dysplasia.

📊

Negative

No pathogenic variants detected in LBR gene.

📊

Variant of Uncertain Significance

Genetic variant found but clinical significance is unknown; further testing may be needed.

⚠️ When to Consult a Doctor:

If symptoms of skeletal dysplasia are present, such as short stature or bone abnormalities, or if there is a family history of the condition.

Frequently Asked Questions

What is the LBR Gene Greenberg Skeletal Dysplasia NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the LBR gene, which is associated with Greenberg skeletal dysplasia.
How much does the test cost?
The test costs INR 20,000 at DNA Labs India.
What sample is required for the test?
The test can be performed on blood, extracted DNA, or one drop of blood on an FTA card.
How long does it take to get results?
Results are typically available in 3-4 weeks.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across India.
What are the symptoms of skeletal dysplasia?
Symptoms include short stature, abnormal bone shape, bowed limbs, joint pain, breathing difficulties, hearing loss, vision problems, and heart defects.
How is skeletal dysplasia diagnosed?
Diagnosis involves physical examination, X-rays, and genetic testing to detect mutations in genes like LBR.
What does a positive result mean?
A positive result indicates a pathogenic variant in the LBR gene, confirming Greenberg skeletal dysplasia.
Is genetic counseling recommended?
Yes, genetic counseling is recommended before and after testing to understand implications and family planning.
Can the test be done for prenatal diagnosis?
Consult a healthcare provider; prenatal testing may be possible but requires specialized consultation.
What are the risks of the test?
The test involves minimal risks, such as discomfort from blood draw, but is generally safe.
How accurate is the NGS technology?
NGS technology is highly accurate for detecting genetic mutations, but results should be interpreted by a qualified professional.
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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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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