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LAS1L Gene Wilson-Turner syndrome NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

LAS1L Gene Wilson-Turner syndrome NGS Genetic Test

Also known as: Wilson-Turner Syndrome Genetic Test, LAS1L Gene Mutation Analysis

LAS1L Gene Wilson-Turner 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 3-4 weeks. Free home collection in 300+ cities across India.

Next-Generation Sequencing (NGS) Genetic TestFemaleAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the LAS1L Gene Wilson-Turner Syndrome NGS Genetic Test is to diagnose Wilson-Turner syndrome by identifying pathogenic mutations in the LAS1L gene, aiding in clinical management, genetic counseling, and informed decision-making for affected individuals and their families.

Test Code
4613
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

A genetic counseling session is recommended to draw a pedigree chart of family members affected with Wilson-Turner syndrome. Clinical history of the patient should be reviewed.

Method: Venipuncture for blood sample

Step 2

Laboratory Analysis

Blood sample is collected via venipuncture, or extracted DNA or one drop of blood on an FTA card is provided.

Step 3

Report Delivery

The sample is sent to the laboratory for NGS analysis, and results are processed and reported.

Timeline: 3-4 weeks

Patient Instructions

1
Before the Test:Genetic counseling and assessment of clinical history and family pedigree.
2
During the Test:Blood sample collection via venipuncture or alternative methods as specified.
3
After the Test:Wait for results (3-4 weeks) and schedule a follow-up with a healthcare provider for interpretation and next steps.

About This Test

Who Should Get This Test

The purpose of the LAS1L Gene Wilson-Turner Syndrome NGS Genetic Test is to diagnose Wilson-Turner syndrome by identifying pathogenic mutations in the LAS1L gene, aiding in clinical management, genetic counseling, and informed decision-making for affected individuals and their families.

How to Prepare

  • Ensure proper sample labeling with patient details
  • Follow aseptic techniques during blood collection
  • Store samples at ambient room temperature if not processed immediately

Doctor's Notes

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

"This test is essential for diagnosing Wilson-Turner syndrome in females presenting with developmental delays, intellectual disabilities, and distinctive facial features, enabling early intervention and genetic counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Blood samples stable at room temperature for up to 24 hours
Extracted DNA stable at -20°C for long-term storage
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results from the LAS1L Gene NGS Genetic Test indicate the presence or absence of mutations in the LAS1L gene associated with Wilson-Turner syndrome. Interpretation should be done by a qualified geneticist or healthcare provider.
Positive result: Pathogenic mutation detected in the LAS1L gene, consistent with a diagnosis of Wilson-Turner syndrome
Negative result: No pathogenic variants detected, but clinical symptoms may warrant further testing or evaluation
Variant of uncertain significance (VUS): Genetic change identified but not clearly linked to disease; requires follow-up
⚠️ When to Consult a Doctor:

Consult a healthcare provider if symptoms of Wilson-Turner syndrome are present, for genetic counseling, or to discuss test results and management options.

Limitations

  • Test only detects mutations in the LAS1L gene
  • May not identify all genetic variations or epigenetic factors
  • Results require clinical correlation for diagnosis

Risks & Considerations

  • Minimal risks from blood draw, such as bruising or infection
  • Potential emotional impact of genetic test results

Interfering Factors

  • Poor sample quality or contamination
  • Insufficient DNA quantity
  • Technical errors during sequencing

Frequently Asked Questions

What is Wilson-Turner syndrome?
Wilson-Turner syndrome is a rare genetic disorder that affects only females, caused by mutations in the LAS1L gene on the X chromosome, leading to developmental delays, intellectual disabilities, and distinctive facial features.
How is the LAS1L Gene NGS Genetic Test performed?
The test uses Next-Generation Sequencing (NGS) technology to analyze the entire coding region of the LAS1L gene from a blood or DNA sample to detect mutations.
What is the cost of the LAS1L Gene NGS Genetic Test?
The test costs INR 20,000 at DNA Labs India, with free home sample collection available across India.
Who should consider this test?
This test is recommended for females with symptoms such as developmental delays, intellectual disabilities, distinctive facial features, or a family history of Wilson-Turner syndrome.
What sample is required for the test?
The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
How long does it take to get results?
Results are typically available within 3-4 weeks after sample collection.
Is fasting required before the test?
No, fasting is not required for this genetic test.
What do the test results mean?
Results indicate whether pathogenic mutations in the LAS1L gene are detected. A positive result suggests Wilson-Turner syndrome, while a negative result may require further clinical evaluation.
Is the test covered by insurance?
Coverage depends on the insurance provider and policy. It is advisable to check with your insurer for specific details.
Can the test be done at home?
Yes, DNA Labs India offers free home sample collection for online bookings across many cities in India.
What are the limitations of this test?
The test only detects mutations in the LAS1L gene and may not identify all genetic variations. Results should be interpreted in conjunction with clinical findings.
How can I prepare for genetic counseling?
Prepare by gathering family medical history and discussing symptoms with a healthcare provider. A genetic counselor will help draw a pedigree chart and explain test implications.
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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Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

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