Loading...

EPIDERMOLYSIS BULLOSA GENE PANEL BY NGS, EDTA BLOOD

image not found

NABL Cap Accredited 
The Ectodermal Dysplasia Gene Panel by NGS is a comprehensive genetic test designed to identify mutations linked to various forms of ectodermal dysplasia. Using advanced next-generation sequencing on EDTA blood, it helps detect inherited conditions affecting hair, teeth, nails, sweat glands, and skin. This test supports early diagnosis, personalized management, and genetic counseling for affected individuals and families.

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 21,000.00

Sample Type: EDTA BLOOD

Fasting Not Required


Frequently Asked Questions (FAQ's):

What does the Ectodermal Dysplasia Gene Panel test include?
It analyzes multiple genes associated with different types of ectodermal dysplasia using NGS technology.

Who should consider this test?
Individuals with symptoms like abnormal hair, teeth, nails, or sweat gland function, or those with a family history of the condition.

How is the sample collected?
A blood sample collected in an EDTA vial is used for genetic analysis.

Can this test confirm a diagnosis?
Yes, it can identify gene mutations that help confirm specific forms of ectodermal dysplasia.

How accurate is this panel?
NGS-based testing provides high sensitivity for detecting pathogenic gene variants.

Does this test help with treatment planning?
It can guide clinical management, supportive care, and long-term monitoring based on the genetic findings.

Is genetic counseling recommended?
Yes, counseling can help families understand the results and inheritance patterns.

How long does it take to receive results?
Turnaround time typically follows standard NGS reporting timelines.

OUR corporates PARTNER

Feedback

Patient's Testimonials

Trusted by Thousands

OUR Accreditations

OUR Lab