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NIN Gene Seckel syndrome type 7 NGS Genetic Test

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NIN Gene Seckel syndrome type 7 NGS Genetic Test

Short Name: NIN Gene Seckel Syndrome Type 7 Test

Also known as: Seckel syndrome type 7, NIN gene Seckel syndrome, Seckel syndrome type 7 genetic test

NIN Gene Seckel syndrome type 7 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses 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 TestPediatric🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr Pasupathy Arumugam

Dr Pasupathy Arumugam

Consultant Pathologist · Reg: 21521

Last reviewed: September 7, 2026

Overview

The purpose of the NIN Gene Seckel Syndrome Type 7 NGS Genetic Test is to detect mutations in the NIN gene responsible for Seckel syndrome type 7. This test aids in confirming diagnosis, guiding treatment plans, and providing genetic counseling for affected individuals and their families.

Test Code
2807
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
NGS
Step 1

Sample Collection

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

Method: Venipuncture or FTA Card

Step 2

Laboratory Analysis

A blood sample will be collected via venipuncture or using an FTA card with one drop of blood.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Store samples at ambient room temperature.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Undergo genetic counseling and provide detailed clinical and family history.
2
During the Test:Sample collection is quick and minimally invasive, typically taking a few minutes.
3
After the Test:Wait for results (3-4 weeks) and schedule a follow-up for interpretation and counseling.

About This Test

Who Should Get This Test

The purpose of the NIN Gene Seckel Syndrome Type 7 NGS Genetic Test is to detect mutations in the NIN gene responsible for Seckel syndrome type 7. This test aids in confirming diagnosis, guiding treatment plans, and providing genetic counseling for affected individuals and their families.

How to Prepare

  • Ensure proper identification of the patient
  • Use sterile collection equipment
  • Label samples correctly
  • Transport samples at ambient temperature

Doctor's Notes

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

"Genetic testing for Seckel syndrome type 7 is essential for accurate diagnosis, family planning, and early intervention. Consult a genetic counselor for personalized guidance."

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 samples stable for 24 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or contaminated samples
  • Incorrect labeling or insufficient sample volume

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the NIN gene. A positive result confirms Seckel syndrome type 7, while a negative result may require further testing if clinical suspicion remains.
📊

No pathogenic variants detected

Normal result; no mutations in NIN gene associated with Seckel syndrome type 7

📊

Pathogenic variants detected

Abnormal result; confirms diagnosis of Seckel syndrome type 7; genetic counseling recommended

⚠️ When to Consult a Doctor:

Consult a doctor or genetic specialist if symptoms of Seckel syndrome are present, after receiving test results, or for family planning advice.

Limitations

  • ⚠May not detect all types of mutations in the NIN gene
  • ⚠Results require interpretation by a genetic specialist
  • ⚠Does not rule out other genetic disorders

Risks & Considerations

  • ●Minimal risks from blood draw, such as bruising or infection
  • ●Emotional impact of genetic results

Frequently Asked Questions

What is Seckel syndrome type 7?
Seckel syndrome type 7 is a rare genetic disorder caused by mutations in the NIN gene, characterized by microcephaly, growth retardation, intellectual disability, and facial abnormalities.
How is the NIN Gene Seckel Syndrome Type 7 test performed?
The test uses Next Generation Sequencing (NGS) to analyze the NIN gene from a blood or DNA sample, identifying mutations associated with the syndrome.
What is the cost of the test in India?
The cost is INR 20000, which includes sample collection, genetic analysis, and report generation.
Is home sample collection available?
Yes, free home collection is available across many cities in India for online bookings.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What sample type is required?
Blood, extracted DNA, or one drop of blood on an FTA card can be used.
Is fasting required before the test?
No, fasting is not required for this genetic test.
Who should consider this test?
Individuals with symptoms like microcephaly, growth retardation, intellectual disability, or a family history of Seckel syndrome should consider testing.
What do the results mean?
A positive result confirms Seckel syndrome type 7, while a negative result may indicate no mutations in the NIN gene, but further evaluation might be needed.
Is genetic counseling provided?
Yes, a genetic counseling session is included to draw a family pedigree chart and discuss implications.
Can this test be used for prenatal diagnosis?
Consult a genetic specialist; prenatal testing may be possible but requires specific procedures.
What are the risks of the test?
Risks are minimal, primarily related to blood draw, such as bruising. Emotional support is available for result interpretation.
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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For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

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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