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CYP24A1 Gene Hypercalcemia infantile type NGS Genetic Test

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CYP24A1 Gene Hypercalcemia infantile type NGS Genetic Test

CYP24A1 Gene Hypercalcemia infantile type 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 TestInfants🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose hypercalcemia infantile type by detecting mutations in the CYP24A1 gene using NGS technology.

Test Code
4695
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

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

Step 2

Laboratory Analysis

Your sample is analyzed using NGS Technology in our laboratory.

Step 3

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

1
Before the Test:Genetic counseling and clinical history review.
2
During the Test:Blood sample collection.
3
After the Test:Wait for report in 3 to 4 weeks.

About This Test

Who Should Get This Test

To diagnose hypercalcemia infantile type by detecting mutations in the CYP24A1 gene using NGS technology.

Doctor's Notes

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

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card

Understanding Your Results

Results indicate the presence or absence of mutations in the CYP24A1 gene associated with hypercalcemia infantile type.
📊

Pathogenic variant detected

Confirms diagnosis of hypercalcemia infantile type. Consult a healthcare professional for management.

📊

No pathogenic variant detected

Unlikely to have hypercalcemia infantile type due to CYP24A1 mutations. Consider other causes if symptoms persist.

⚠️ When to Consult a Doctor:

If symptoms of hypercalcemia are present, such as weakness, vomiting, or kidney stones, consult a healthcare professional for evaluation and testing.

Risks & Considerations

  • Minimal risk from blood draw
  • Genetic counseling recommended for emotional impact

Frequently Asked Questions

What is the CYP24A1 Gene Hypercalcemia Infantile Type NGS Genetic Test?
It is a genetic test that uses Next Generation Sequencing to detect mutations in the CYP24A1 gene, which causes hypercalcemia infantile type, a rare disorder leading to high calcium levels in infants.
What are the symptoms of hypercalcemia infantile type?
Symptoms include weakness, fatigue, poor feeding, vomiting, dehydration, constipation, abdominal pain, frequent urination, kidney stones, and bone pain, often appearing in the first few months of life.
How is hypercalcemia infantile type diagnosed?
Diagnosis is primarily through genetic testing like the NGS Genetic Test for CYP24A1 gene mutations, supplemented by blood tests to measure calcium levels and urine tests.
What is the cost of the test in India?
The cost is INR 20,000, with free home sample collection available across India.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in numerous cities across India.
How long does it take to get the results?
Reports are typically delivered in 3 to 4 weeks via online portal, email, or WhatsApp.
What does a positive test result mean?
A positive result indicates the presence of pathogenic mutations in the CYP24A1 gene, confirming hypercalcemia infantile type. Consult a healthcare professional for management.
Can this test be done for adults?
The test is primarily for infants with symptoms, but adults with a family history or symptoms may also be tested after genetic counseling.
Is genetic counseling required before the test?
Yes, a genetic counseling session is recommended to draw a pedigree chart and discuss implications before testing.
What treatments are available for hypercalcemia infantile type?
Treatment includes fluids, electrolytes, medications to lower calcium, vitamin D supplements, and genetic counseling, as there is no cure.
Is the test covered by insurance?
Coverage varies; it is not typically covered under government schemes like PMJAY or CGHS, but check with private insurers.
How accurate is the NGS genetic test?
NGS is highly accurate for detecting gene mutations, but accuracy depends on sample quality and laboratory standards. DNA Labs India follows stringent protocols.
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 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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