KRT17 Gene Steatocystoma multiplex NGS Genetic Test
Short Name: KRT17 Steatocystoma Multiplex Test
Also known as: KRT17 gene test for steatocystoma multiplex, Steatocystoma multiplex genetic diagnosis
KRT17 Gene Steatocystoma multiplex 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 SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of the KRT17 Gene Steatocystoma Multiplex NGS Genetic Test is to detect mutations in the KRT17 gene responsible for steatocystoma multiplex, enabling accurate diagnosis, genetic counseling, and informed clinical management. It helps differentiate this condition from other cystic skin disorders and provides insights for family risk assessment.
- Test Code
- 5141
- 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
No specific preparation required. Provide clinical history and undergo genetic counseling session to draw a pedigree chart.
Method: Venipuncture
Laboratory Analysis
A blood sample will be collected via venipuncture or a saliva sample may be used. The process is non-invasive and painless.
Report Delivery
Apply pressure to the puncture site to prevent bleeding. Store sample as instructed for stability.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the KRT17 Gene Steatocystoma Multiplex NGS Genetic Test is to detect mutations in the KRT17 gene responsible for steatocystoma multiplex, enabling accurate diagnosis, genetic counseling, and informed clinical management. It helps differentiate this condition from other cystic skin disorders and provides insights for family risk assessment.
How to Prepare
- Ensure proper identification of patient
- Use sterile collection equipment
- Label sample correctly with patient details
- Transport sample at ambient room temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for confirming genetic mutations in suspected cases of steatocystoma multiplex, aiding in accurate diagnosis and family counseling for hereditary skin conditions."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted sample
- Insufficient sample volume
- Incorrect sample labeling
- Contaminated sample
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of steatocystoma multiplex due to KRT17 mutation. Genetic counseling recommended.
No pathogenic variant detected
Steatocystoma multiplex unlikely due to KRT17 mutation. Consider other causes or repeat testing if clinically indicated.
Variant of uncertain significance
Further testing or family studies may be needed. Consult a geneticist for guidance.
Consult a healthcare professional if you have multiple skin cysts, family history of steatocystoma multiplex, or symptoms like itching and inflammation. After receiving test results, seek genetic counseling for interpretation and management.
Limitations
- ⚠May not detect all possible mutations in the KRT17 gene
- ⚠Requires genetic counseling for interpretation
- ⚠Results should be correlated with clinical findings
- ⚠Not a substitute for clinical examination in all cases
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising or infection
- ●Psychological impact of genetic results
- ●No significant risks from the test itself
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
- ●Hemolyzed blood sample
- ●Improper sample storage
Compare With Similar Tests
| Test | KRT17 Gene Steatocystoma multiplex NGS Genetic Test | Skin Biopsy | Clinical Examination | Other Genetic Tests |
|---|---|---|---|---|
| Comparison | KRT17 Gene Steatocystoma multiplex NGS Genetic Test |
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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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