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KRT71 Gene Hypotrichosis type 13 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

KRT71 Gene Hypotrichosis type 13 NGS Genetic Test

Short Name: KRT71 Hypotrichosis NGS Test

Also known as: Hypotrichosis Type 13, KRT71-related hypotrichosis, Autosomal recessive hypotrichosis

KRT71 Gene Hypotrichosis type 13 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.

NGS Genetic Test🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

To diagnose mutations in the KRT71 gene causing hypotrichosis type 13, enabling early management, genetic counseling, and family planning.

Test Code
4980
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
Step 1

Sample Collection

No specific preparation required. Provide clinical history and family pedigree if available.

Method: Venipuncture or Saliva

Step 2

Laboratory Analysis

A small blood sample or saliva sample will be collected by a trained professional.

Step 3

Report Delivery

Apply pressure to the puncture site if blood is drawn. Store sample as instructed.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Provide detailed clinical and family history. Genetic counseling session may be recommended.
2
During the Test:Sample collection is quick and minimally invasive. No special procedures required.
3
After the Test:Wait for results as per turnaround time. Follow up with healthcare provider for interpretation.

About This Test

Who Should Get This Test

To diagnose mutations in the KRT71 gene causing hypotrichosis type 13, enabling early management, genetic counseling, and family planning.

How to Prepare

  • Ensure sample is collected in a sterile container
  • Label sample with patient details
  • Transport to lab within specified stability period

Doctor's Notes

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

"Early genetic testing for hypotrichosis can guide management and family planning, especially for couples with a family history of genetic disorders."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or Saliva

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Improper labeling or contamination

Understanding Your Results

Results indicate the presence or absence of mutations in the KRT71 gene. Genetic counseling is recommended for understanding implications.
📊

Pathogenic variant detected

Confirms diagnosis of hypotrichosis type 13. Genetic counseling and management recommended.

📊

No pathogenic variant detected

KRT71 gene mutations not found. Consider other genetic or non-genetic causes.

📊

Variant of uncertain significance

Further testing or family studies may be needed for clarification.

⚠️ When to Consult a Doctor:

Consult a geneticist or dermatologist if symptoms persist, for family planning, or after receiving test results for management guidance.

Limitations

  • ⚠May not detect all possible mutations in the KRT71 gene
  • ⚠Requires genetic counseling for interpretation
  • ⚠Results may not predict disease severity

Risks & Considerations

  • ●Minimal risk from blood draw, such as bruising or infection
  • ●Psychological impact of genetic diagnosis

Interfering Factors

  • ●Sample contamination
  • ●Improper storage or handling
  • ●Degraded DNA

Compare With Similar Tests

TestKRT71 Gene Hypotrichosis type 13 NGS Genetic TestSanger Sequencing for KRT71Comprehensive Hair Disorder Gene PanelSkin Biopsy
ComparisonKRT71 Gene Hypotrichosis type 13 NGS Genetic Test

Frequently Asked Questions

What is KRT71 Gene Hypotrichosis Type 13?
It is a rare genetic disorder caused by mutations in the KRT71 gene, leading to sparse hair or hair loss, scaly skin, and brittle nails.
What are the symptoms of this condition?
Symptoms include sparse hair or alopecia, thick scaly scalp skin, brittle nails, and increased risk of skin infections, often appearing in early childhood.
How is the test performed?
The test uses NGS technology to analyze DNA from a blood or saliva sample for mutations in the KRT71 gene.
What is the cost of the test?
The cost is INR 20,000, which includes sample collection, lab analysis, and result interpretation.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection across many cities in India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the results mean?
Results indicate if pathogenic mutations are present in the KRT71 gene, confirming or ruling out the diagnosis.
Is the test painful?
No, the test involves a simple blood draw or saliva collection, which is minimally invasive.
Can this test be done for children?
Yes, the test can be performed on individuals of all ages, including children, with appropriate consent.
What are the treatment options after diagnosis?
Treatment focuses on symptom management, such as topical treatments for skin issues and protective measures for hair loss. Genetic counseling is recommended.
Is genetic counseling recommended?
Yes, genetic counseling is advised to understand the implications, family risk, and management options.
How accurate is the NGS Genetic Test?
NGS is highly accurate for detecting mutations, but results should be interpreted by a qualified geneticist in clinical context.
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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