KINDLER SYNDROME (FERMT1) GENE SEQUENCING
A test to detect mutations in the FERMT1 gene, which causes Kindler syndrome, a rare genetic disorder affecting the skin and mucous membranes.
Also known asKindler Syndrome (fermt1) Gene Sequencing Kindler Syndrome (fermt1) Gene Sequencing
Test details
Preparations
No special preparations needed
Test included
KINDLER SYNDROME (FERMT1) GENE SEQUENCING includes 1 parameter
- Specimen
Test code
G688
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Others (fx) | Others | 2 ML |
Specimen stability information
Others (Fx)
Specimen rejection criteria
Test run frequency
Every Day TIME - 10:00
Turn around time
28 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
KINDLER SYNDROME (FERMT1) GENE SEQUENCING
Package price
₹22000
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₹22000