LORICRIN Gene Vohwinkel syndrome with ichthyosis NGS Genetic Test
Also known as: Vohwinkel Syndrome with Ichthyosis
LORICRIN Gene Vohwinkel syndrome with ichthyosis NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of the LORICRIN Gene Vohwinkel Syndrome with Ichthyosis NGS Genetic Test is to diagnose Vohwinkel Syndrome with Ichthyosis by detecting mutations in the LORICRIN gene using Next-Generation Sequencing (NGS) technology, aiding in clinical management and genetic counseling.
- Test Code
- 5165
- 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 Technology
Sample Collection
Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Vohwinkel Syndrome with Ichthyosis are required before sample collection.
Method: Venipuncture
Laboratory Analysis
Your sample is analyzed using NGS Technology in our laboratory.
Report Delivery
A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the LORICRIN Gene Vohwinkel Syndrome with Ichthyosis NGS Genetic Test is to diagnose Vohwinkel Syndrome with Ichthyosis by detecting mutations in the LORICRIN gene using Next-Generation Sequencing (NGS) technology, aiding in clinical management and genetic counseling.
How to Prepare
- Collect blood sample via venipuncture or use extracted DNA or one drop of blood on an FTA card.
- Ensure proper labeling and handling of samples.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Early diagnosis through genetic testing can help manage symptoms and provide family counseling for Vohwinkel Syndrome with Ichthyosis."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
No mutation detected
Negative for LORICRIN gene mutations; clinical correlation recommended.
Mutation detected
Positive for LORICRIN gene mutation; confirms diagnosis of Vohwinkel Syndrome with Ichthyosis.
Consult a doctor if you experience symptoms such as thick, scaly skin, itching, pain, cracks in the skin, nail abnormalities, hearing loss, or vision problems, especially if there is a family history of genetic skin disorders.
Frequently Asked Questions
What is Vohwinkel Syndrome with Ichthyosis?
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₹20,000Reference 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.
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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