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KCTD3 Gene Neurodevelopmental disorder, KCTD3 related NGS Genetic Test

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KCTD3 Gene Neurodevelopmental disorder, KCTD3 related NGS Genetic Test

Short Name: KCTD3 Gene NGS Test

Also known as: KCTD3 Gene Mutation Test, KCTD3 NGS Genetic Test

KCTD3 Gene Neurodevelopmental disorder, KCTD3 related 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.

Next Generation Sequencing (NGS)🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the KCTD3 Gene Neurodevelopmental Disorder NGS Genetic Test is to detect mutations in the KCTD3 gene that cause neurodevelopmental disorders. It aids in accurate diagnosis, helps differentiate from other conditions, informs treatment plans, and provides genetic counseling for family planning.

Test Code
1766
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

Provide clinical history and undergo genetic counseling to draw a pedigree chart of affected family members.

Method: Venipuncture or finger prick for FTA card

Step 2

Laboratory Analysis

A trained phlebotomist will collect a blood sample or assist with FTA card sample preparation.

Step 3

Report Delivery

Apply pressure to the puncture site, keep bandage on, and avoid strenuous activity briefly.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor, provide detailed medical and family history, and ensure sample collection is scheduled.
2
During the Test:Sample collection is minimally invasive; follow instructions from the collection team.
3
After the Test:Results will be available in 3-4 weeks; schedule a follow-up with a healthcare provider to discuss outcomes.

About This Test

Who Should Get This Test

The purpose of the KCTD3 Gene Neurodevelopmental Disorder NGS Genetic Test is to detect mutations in the KCTD3 gene that cause neurodevelopmental disorders. It aids in accurate diagnosis, helps differentiate from other conditions, informs treatment plans, and provides genetic counseling for family planning.

How to Prepare

  • Use an EDTA tube for blood samples
  • For FTA card, use one drop of blood as instructed
  • Ensure proper labeling with patient details
  • Store samples at ambient room temperature unless specified

Doctor's Notes

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

"Genetic testing for KCTD3 mutations is essential for accurate diagnosis of neurodevelopmental disorders and can guide family planning and management strategies."

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 of blood or appropriate DNA amount
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or finger prick for FTA card

Sample Stability

Blood: Stable for 48 hours at room temperature
Extracted DNA: Stable for years if stored at -20°C or below
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Improperly labeled or contaminated sample
  • Wrong sample type

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the KCTD3 gene, which is associated with neurodevelopmental disorders.
Positive: Pathogenic variant detected, supporting diagnosis of KCTD3-related neurodevelopmental disorder
Negative: No pathogenic variants detected, but does not rule out other causes
Variant of Uncertain Significance (VUS): Variant found but clinical significance unknown; further testing or family studies may be needed
⚠️ When to Consult a Doctor:

If symptoms of neurodevelopmental disorder are present, or if there is a family history, consult a healthcare provider for genetic testing and counseling.

Limitations

  • May not detect all types of genetic variants (e.g., deep intronic mutations)
  • Requires interpretation by a genetic specialist
  • Not diagnostic for all causes of neurodevelopmental disorders
  • Variant of uncertain significance (VUS) may be identified

Risks & Considerations

  • Minor bruising or discomfort at needle site
  • Rare risk of infection
  • Dizziness or fainting during blood draw

Interfering Factors

  • Sample degradation
  • Contamination during collection
  • Incorrect sample type or handling

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Frequently Asked Questions

What is KCTD3 gene neurodevelopmental disorder?
It is a rare genetic condition caused by mutations in the KCTD3 gene, leading to neurodevelopmental issues such as intellectual disability and speech delays.
What are the common symptoms?
Symptoms include delayed speech, intellectual disability, motor delays, behavioral problems, epilepsy, and autistic features.
How is the disorder diagnosed?
Diagnosis is primarily through genetic testing, like NGS, to identify mutations in the KCTD3 gene, combined with clinical evaluation.
What is NGS genetic testing?
Next Generation Sequencing (NGS) is a high-throughput method that analyzes multiple genes simultaneously to detect genetic variations.
What is the cost of the test in India?
The cost is typically INR 20,000 at DNA Labs India, with discounts available for online bookings.
Is the test covered by insurance?
Genetic testing is not always covered by insurance; check with your provider for specific coverage details.
How long does it take to get results?
Results are usually available within 3 to 4 weeks after sample collection.
What sample is required?
A blood sample, extracted DNA, or one drop of blood on an FTA card can be used.
Is home collection available?
Yes, DNA Labs India offers free home sample collection across many cities in India.
What should I do before the test?
Provide clinical history and attend a genetic counseling session to discuss family history and testing implications.
How accurate is the genetic test?
NGS is highly accurate for detecting mutations, but interpretation requires expertise, and some variants may be of uncertain significance.
What are the treatment options?
There is no cure; management focuses on symptom relief, therapy, and support services tailored to the individual's needs.
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 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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