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OSMR Gene Amyloidosis, primary localized cutaneous, type 1 NGS Genetic Test

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OSMR Gene Amyloidosis, primary localized cutaneous, type 1 NGS Genetic Test

Short Name: OSMR Gene Amyloidosis NGS Test

Also known as: Primary Localized Cutaneous Amyloidosis Type 1, OSMR-related Amyloidosis

OSMR Gene Amyloidosis, primary localized cutaneous, type 1 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.

Dermatologist🏠 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

To detect mutations in the OSMR gene for diagnosis of primary localized cutaneous amyloidosis type 1.

Test Code
4841
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 and undergo genetic counseling.

Method: Venipuncture for blood, or provided FTA card

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or use of FTA card.

Step 3

Report Delivery

Sample sent to lab for NGS analysis.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review.
2
During the Test:Sample collection and preparation for NGS.
3
After the Test:Report generation and consultation for results.

About This Test

Who Should Get This Test

To detect mutations in the OSMR gene for diagnosis of primary localized cutaneous amyloidosis type 1.

How to Prepare

  • Ensure proper sample labeling
  • Avoid hemolysis in blood samples
  • Store samples as per guidelines

Doctor's Notes

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

"Genetic testing for OSMR mutations is crucial for confirming diagnosis and guiding management in suspected cases of primary localized cutaneous amyloidosis."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
ContainerAppropriate container for blood or DNA
Collection MethodVenipuncture for blood, or provided FTA card

Sample Stability

Blood samples stable for 48 hours at room temperature
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient volume
  • Contaminated samples

Understanding Your Results

Results indicate presence or absence of pathogenic mutations in the OSMR gene.
📊

Positive

Pathogenic mutation detected; confirms diagnosis.

📊

Negative

No mutation detected; clinical correlation advised.

⚠️ When to Consult a Doctor:

If symptoms persist or worsen, consult a geneticist or dermatologist.

Limitations

  • ⚠May not detect all mutations; clinical correlation required.

Risks & Considerations

  • ●Psychological impact
  • ●Incidental findings

Interfering Factors

  • ●Degraded DNA
  • ●Sample contamination

Compare With Similar Tests

TestOSMR Gene Amyloidosis, primary localized cutaneous, type 1 NGS Genetic TestSkin BiopsyBlood Tests
ComparisonOSMR Gene Amyloidosis, primary localized cutaneous, type 1 NGS Genetic TestInvasive, histological analysis vs. genetic mutation detection.General markers vs. specific gene sequencing.

Frequently Asked Questions

What is OSMR Gene Amyloidosis?
It is a rare genetic disorder caused by mutations in the OSMR gene, leading to skin and sometimes systemic symptoms.
What are the common symptoms?
Symptoms include thickened skin, itching, red spots, non-healing lesions, joint pain, and swelling.
How is it diagnosed?
Diagnosis involves skin biopsy, blood tests, genetic testing, and imaging like X-rays or MRI.
What is the NGS Genetic Test?
It is a next-generation sequencing test that detects mutations in the OSMR gene for accurate diagnosis.
What is the cost of the test in India?
The test costs INR 20000 at DNA Labs India.
Is home sample collection available?
Yes, free home collection is available across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What sample is required?
Blood, extracted DNA, or one drop of blood on an FTA card.
Is fasting required before the test?
No, fasting is not required.
Who should consider this test?
Individuals with symptoms of primary localized cutaneous amyloidosis or a family history.
What are the risks of genetic testing?
Risks include psychological impact and potential incidental findings.
How can I book the test?
Book online via DNA Labs India's website or contact their helpline.
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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✓ 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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