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FH Genetic Testing Patient Testing Requisition FormProgenika Diagnostic Services CIA Certified & CAP AccreditedPatient Information Last nameProvider Information First nameMiddle nameRequesting Provider

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What is fh genetic testing?

FH genetic testing is a type of genetic test that looks for mutations in the genes that cause familial hypercholesterolemia (FH), a genetic disorder that causes high levels of low-density lipoprotein (LDL) cholesterol.

Who is required to file fh genetic testing?

Individuals who suspect that they may have FH or have a family history of FH may be required to undergo FH genetic testing.

How to fill out fh genetic testing?

FH genetic testing is typically done through a blood sample or a saliva sample. The sample is sent to a laboratory for analysis, and the results are reported back to the healthcare provider who ordered the test.

What is the purpose of fh genetic testing?

The purpose of FH genetic testing is to identify mutations in the genes that cause FH, which can help in diagnosing the condition and guiding treatment decisions.

What information must be reported on fh genetic testing?

The results of the genetic test, including any mutations found in the genes associated with FH, must be reported on FH genetic testing.

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