Cowden syndrome laboratory findings
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]
Overview
Laboratory findings consistent with the diagnosis of cowden syndrome include skin biopsy, chemistry panels, urinalysis, thyroid function tests and cbc count.
Laboratory Findings
Laboratory findings consistent with the diagnosis of cowden syndrome include:
Gene testing
- PTEN mutation testing by following:
- Sequence analysis of coding region
- Deletion/duplication analysis
- Sequence analysis of promoter region