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FASLG Gene Autoimmune lymphoproliferative syndrome type 1B NGS Genetic Test

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FASLG Gene Autoimmune lymphoproliferative syndrome type 1B NGS Genetic Test

Short Name: FASLG Gene ALPS Type 1B NGS Test

Also known as: ALPS Type 1B Genetic Test, FASLG Mutation Analysis, Autoimmune Lymphoproliferative Syndrome Type 1B Test

FASLG Gene Autoimmune lymphoproliferative syndrome type 1B 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 to 4 Weeks. Free home collection in 300+ cities across India.

NGS Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to detect mutations in the FASLG gene that cause Autoimmune Lymphoproliferative Syndrome Type 1B. It aids in confirming diagnosis, understanding disease prognosis, and guiding therapeutic interventions such as immunosuppressive therapy and monitoring for autoimmune complications or lymphoma.

Test Code
2370
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
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation required. Provide clinical history and family pedigree as per pre-test information.

Method: Venipuncture or FTA Card

Step 2

Laboratory Analysis

A blood sample is drawn from a vein or a saliva sample is collected using standard protocols.

Step 3

Report Delivery

Apply pressure to the puncture site if blood is drawn. No special aftercare is typically needed.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Undergo a genetic counseling session to discuss test implications, draw a pedigree chart, and provide informed consent.
2
During the Test:DNA extraction from the sample followed by Next-Generation Sequencing to analyze the FASLG gene for mutations.
3
After the Test:Review results with a genetic counselor and physician to understand diagnosis, treatment options, and family implications.

About This Test

Who Should Get This Test

The purpose of this test is to detect mutations in the FASLG gene that cause Autoimmune Lymphoproliferative Syndrome Type 1B. It aids in confirming diagnosis, understanding disease prognosis, and guiding therapeutic interventions such as immunosuppressive therapy and monitoring for autoimmune complications or lymphoma.

How to Prepare

  • Bring identification and doctor's referral
  • Avoid certain medications if advised by the physician
  • Ensure proper labeling of samples

Doctor's Notes

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

"This genetic test is essential for confirming ALPS Type 1B diagnosis, guiding immunosuppressive therapy, and monitoring for complications like lymphoma. Early detection can improve patient outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Blood sample: stable for 48 hours at room temperature
Extracted DNA: stable for several days at 4°C
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient sample volume
  • Incorrect sample container or labeling

Understanding Your Results

Results indicate the presence or absence of mutations in the FASLG gene. Genetic counseling is recommended for understanding the implications, inheritance patterns, and management options.
📊

Pathogenic variant detected

Confirms diagnosis of ALPS Type 1B. Guide treatment with immunosuppressive therapy and recommend family screening.

📊

No pathogenic variant detected

ALPS Type 1B is unlikely. Consider other genetic or clinical causes for symptoms.

📊

Variant of uncertain significance

Further testing, family studies, or clinical correlation may be needed for clarification.

⚠️ When to Consult a Doctor:

If symptoms of ALPS such as enlarged lymph nodes, recurrent infections, or autoimmune disorders persist, or if there is a family history of ALPS, consult a geneticist or immunologist promptly.

Limitations

  • May not detect all genetic variants
  • Requires genetic counseling for interpretation
  • Does not cover other ALPS-related genes

Risks & Considerations

  • Minimal physical risk from blood draw, such as bruising or infection
  • Potential psychological impact of genetic results, including anxiety
  • Risk of incidental findings unrelated to ALPS

Interfering Factors

  • Sample contamination
  • Insufficient DNA quality
  • Technical errors during sequencing

Compare With Similar Tests

TestFASLG Gene Autoimmune lymphoproliferative syndrome type 1B NGS Genetic Test
ComparisonFASLG Gene Autoimmune lymphoproliferative syndrome type 1B NGS Genetic Test

Frequently Asked Questions

What is ALPS Type 1B?
ALPS Type 1B is a rare genetic subtype of Autoimmune Lymphoproliferative Syndrome caused by mutations in the FASLG gene, leading to immune dysregulation and autoimmune symptoms.
How is ALPS Type 1B diagnosed?
Diagnosis involves clinical evaluation of symptoms and genetic testing, such as NGS, to identify mutations in the FASLG gene.
What does the FASLG gene test involve?
The test uses Next-Generation Sequencing to analyze DNA from a blood or saliva sample for mutations in the FASLG gene.
What is the cost of the FASLG Gene ALPS Type 1B NGS Test in India?
The test costs INR 20000 at DNA Labs India, with home sample collection available across India.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What if the test is positive for a mutation?
A positive result confirms ALPS Type 1B, guiding treatment with immunosuppressive therapy and recommending family screening.
Can this test be done for children?
Yes, the test can be performed on individuals of all ages, including children, with appropriate consent and counseling.
Is the test covered by insurance?
Coverage depends on the insurance provider and policy; check with your insurer for details.
What are the symptoms of ALPS Type 1B?
Symptoms include enlarged lymph nodes, spleen, and liver, recurrent infections, and autoimmune disorders like hemolytic anemia or thrombocytopenia.
How accurate is NGS testing for ALPS Type 1B?
NGS is highly accurate for detecting gene mutations, but genetic counseling is recommended for interpretation due to possible variants of uncertain significance.
What is the next step after diagnosis?
After diagnosis, consult a specialist for personalized treatment, which may include immunosuppressive drugs, monitoring, and family planning advice.
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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