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WNT4 Gene SERKAL syndrome NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

WNT4 Gene SERKAL syndrome NGS Genetic Test

Short Name: SERKAL Syndrome NGS Test

Also known as: WNT4-related syndrome

WNT4 Gene SERKAL 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 TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the WNT4 Gene SERKAL Syndrome NGS Genetic Test is to detect mutations in the WNT4 gene, enabling accurate diagnosis of SERKAL Syndrome. This helps in confirming the condition, guiding clinical management, and providing genetic counseling for affected individuals and their families.

Test Code
2647
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

Clinical history review and genetic counseling session recommended to draw a pedigree chart of affected family members.

Method: Blood Draw or FTA Card

Step 2

Laboratory Analysis

Standard blood draw via venipuncture or collection using an FTA card, following sterile techniques.

Step 3

Report Delivery

Sample is labeled, stored at ambient room temperature, and transported to the laboratory for analysis.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical evaluation to assess symptoms and family history.
2
During the Test:Sample collection (blood or FTA card) and processing in the laboratory using NGS technology.
3
After the Test:Report generation, delivery via online portal, email, or WhatsApp, followed by consultation with a healthcare provider.

About This Test

Who Should Get This Test

The purpose of the WNT4 Gene SERKAL Syndrome NGS Genetic Test is to detect mutations in the WNT4 gene, enabling accurate diagnosis of SERKAL Syndrome. This helps in confirming the condition, guiding clinical management, and providing genetic counseling for affected individuals and their families.

How to Prepare

  • Ensure proper patient identification and sample labeling
  • Use sterile collection equipment
  • Follow laboratory-specific protocols for blood or FTA card collection
  • Avoid hemolysis during blood draw

Doctor's Notes

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

"Genetic testing is crucial for accurate diagnosis of SERKAL Syndrome to guide management and family planning."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Blood samples stable for up to 48 hours at room temperature
FTA cards stable for extended periods at ambient conditions
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Improper labeling or documentation
  • Contaminated samples

Understanding Your Results

Results from the WNT4 Gene SERKAL Syndrome NGS Genetic Test indicate the presence or absence of pathogenic mutations in the WNT4 gene, which are associated with SERKAL Syndrome.
📊

Pathogenic variant detected

Consistent with a diagnosis of SERKAL Syndrome. Clinical correlation and genetic counseling are recommended.

📊

No pathogenic variant detected

SERKAL Syndrome is unlikely based on genetic analysis, but clinical evaluation should continue if symptoms persist.

📊

Variant of uncertain significance (VUS)

Further testing or family studies may be needed for clarification. Consult a genetic specialist.

⚠️ When to Consult a Doctor:

Consult a doctor if symptoms such as kidney abnormalities, genital anomalies, infertility, or delayed puberty are present, or for family planning advice if there is a family history of SERKAL Syndrome.

Limitations

  • May not detect all types of mutations, such as large deletions or intronic variants
  • Requires genetic counseling for interpretation
  • Results may have psychological or familial implications

Risks & Considerations

  • Minimal risk from blood draw, such as bruising or infection
  • Potential psychological impact of genetic results
  • Implications for family members regarding inheritance

Interfering Factors

  • Sample degradation
  • Contamination during collection or processing
  • Technical errors in sequencing

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ComparisonWNT4 Gene SERKAL syndrome NGS Genetic Test

Frequently Asked Questions

What is SERKAL Syndrome?
SERKAL Syndrome is a rare genetic disorder caused by mutations in the WNT4 gene, affecting the development of kidneys, urinary tract, and external genitalia.
What causes SERKAL Syndrome?
It is caused by mutations in the WNT4 gene, which is involved in organ development during embryonic stages.
What are the common symptoms of SERKAL Syndrome?
Symptoms include abnormalities in kidneys and urinary tract, genital anomalies, infertility, and delayed puberty.
How is SERKAL Syndrome diagnosed?
Diagnosis involves clinical evaluation, imaging studies, and genetic testing, with NGS being the most reliable method.
What is the NGS Genetic Test for SERKAL Syndrome?
It is a Next-Generation Sequencing test that detects mutations in the WNT4 gene to confirm SERKAL Syndrome.
What is the cost of the WNT4 Gene SERKAL Syndrome NGS Genetic Test?
The test costs INR 20000 at DNA Labs India, with home sample collection available.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for online bookings across India.
How long does it take to get the test results?
Results are typically delivered within 3 to 4 weeks via online portal, email, or WhatsApp.
What do the test results indicate?
Results show the presence or absence of WNT4 gene mutations, helping diagnose SERKAL Syndrome and guide management.
Is genetic counseling recommended before or after the test?
Yes, genetic counseling is recommended to understand the implications of results and for family planning.
Can this test be used for prenatal diagnosis?
It may be considered in some cases, but consultation with a genetic specialist is essential for prenatal applications.
What are the risks associated with the genetic test?
Risks are minimal, primarily related to blood draw, but psychological impacts of results should be considered.
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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