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Test Code 8471

Dyskeratosis Congenita (DC) and Revesz Syndrome via the TINF2 Gene

TINF2

N/A

Who is this test for?

Candidates for this test are patients with symptoms consistent with autosomal dominant Dyskeratosis Congenita, Revesz syndrome and the family members of patients who have known TINF2 variants.

Method
Sequencing with CNV PGxome
Specimen(s)

Blood, Saliva, or Buccal Swab

Order Options

Platform
Test type
OTHER OPTIONS
for standard institutional pricing.

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