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CFH Gene Hemolytic uremic syndrome NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

CFH Gene Hemolytic uremic syndrome NGS Genetic Test

Short Name: CFH Gene HUS NGS Test

Also known as: CFH Gene Mutation Test for HUS, Complement Factor H Genetic Test, Atypical HUS Genetic Test

CFH Gene Hemolytic uremic syndrome 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 Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify genetic mutations in the CFH gene associated with Hemolytic Uremic Syndrome (HUS), aiding in diagnosis, personalized treatment planning, and family risk assessment.

Test Code
5412
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

Consult with a healthcare provider or genetic counselor to discuss test implications. No specific preparation is required, but ensure accurate medical history is provided.

Method: Venipuncture or finger-prick

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm or a finger-prick for FTA card collection. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the collection site to prevent bruising. Resume normal activities immediately. Results will be available online in 3-4 weeks.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Schedule a genetic counseling session to understand the test's implications and provide informed consent.
2
During the Test:A small blood sample is collected via venipuncture or finger-prick, taking about 10-15 minutes.
3
After the Test:Results are delivered online within 3-4 weeks. Follow-up with a specialist is recommended for result interpretation.

About This Test

Who Should Get This Test

To identify genetic mutations in the CFH gene associated with Hemolytic Uremic Syndrome (HUS), aiding in diagnosis, personalized treatment planning, and family risk assessment.

How to Prepare

  • Ensure the patient is relaxed and hydrated
  • Use sterile equipment for blood collection
  • Label samples correctly with patient details
  • Store samples at ambient temperature as specified

Doctor's Notes

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

"Genetic testing for CFH gene mutations is crucial for diagnosing atypical HUS and guiding targeted therapies like complement inhibitors, improving patient outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume3-5 mL blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or finger-prick

Sample Stability

Blood sample: Stable for 48 hours at room temperature
Extracted DNA: Stable for years if stored properly
FTA card: Stable for extended periods at room temperature
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Incorrectly labeled or contaminated samples

Understanding Your Results

Results from the CFH Gene HUS NGS Test indicate the presence or absence of mutations in the CFH gene. A positive result suggests a genetic predisposition to atypical HUS, while a negative result may not completely exclude other genetic or non-genetic causes.
📊

No pathogenic variants detected

Normal finding; CFH gene mutations are unlikely to be the cause of HUS symptoms. Further clinical evaluation may be needed.

Action: Consult with a nephrologist for alternative diagnoses.

📊

Pathogenic variant(s) detected

Abnormal finding; indicates a genetic mutation in the CFH gene associated with increased risk of atypical HUS.

Action: Seek genetic counseling and discuss targeted treatments with a specialist.

⚠️ When to Consult a Doctor:

If you experience symptoms like bloody diarrhea, reduced urine output, or unexplained fatigue, or if you have a family history of HUS, consult a nephrologist or genetic counselor promptly.

Limitations

  • May not detect all rare or novel mutations in the CFH gene
  • Results require interpretation by a genetic counselor or specialist
  • Does not rule out other causes of HUS, such as infections or autoimmune disorders

Risks & Considerations

  • Minor pain or bruising at the blood collection site
  • Very low risk of infection or dizziness
  • Potential psychological impact of genetic results

Interfering Factors

  • Recent blood transfusions may affect DNA quality
  • Sample contamination or improper storage
  • Use of certain medications that alter DNA integrity

Frequently Asked Questions

What is the CFH Gene Hemolytic Uremic Syndrome NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to analyze the CFH gene for mutations associated with Hemolytic Uremic Syndrome (HUS), helping diagnose atypical HUS.
Why is this test recommended?
This test is recommended for individuals with symptoms of HUS, family history of the condition, or unexplained kidney failure to identify genetic causes and guide treatment.
What are the symptoms of Hemolytic Uremic Syndrome?
Common symptoms include abdominal pain, bloody diarrhea, fever, fatigue, decreased urine output, and jaundice due to hemolytic anemia.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to sequence the CFH gene and detect any mutations.
What is the cost of the test?
The test costs INR 20000 at DNA Labs India, which includes sample collection and analysis.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test across many cities in India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result indicates a mutation in the CFH gene, suggesting a genetic predisposition to atypical HUS, which may require specialized treatment.
Can children undergo this test?
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 varies by insurance plan; it is advisable to check with your provider. DNA Labs India offers affordable pricing.
How should I prepare for the test?
No special preparation is needed, but consult with a genetic counselor beforehand to discuss implications and provide medical history.
What are the risks of the test?
Risks are minimal, including minor bruising at the blood draw site. Genetic results may have emotional implications, so counseling is recommended.
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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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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