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FAMILIAL HYPERCHOLESTEROLAEMIA RARE DISEASE GENOMIC TEST ORDER FORM PATIENT DETAILS (or address label)ORDERING CLINICIAN INFORMATIONNHS NO.*SUBMITTER HOSPITAL OR GP SURGERY*HOSPITAL NO. FAMILY NO.
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How to fill out case-finding and genetic testing

01
Start by gathering detailed information about the patient's personal and family medical history.
02
Consider any red flags or warning signs that may indicate a genetic condition.
03
Consult with a genetic counselor or healthcare provider to determine the appropriate genetic tests to consider.
04
Obtain informed consent from the patient before proceeding with testing.
05
Collect samples (blood, saliva, etc.) as needed for genetic testing.
06
Send samples to a reputable laboratory for analysis.
07
Review and interpret the test results with the patient and discuss any implications for their health and future care.

Who needs case-finding and genetic testing?

01
Individuals with a personal or family history of genetic conditions or hereditary diseases.
02
People at risk for certain genetic conditions based on their ancestry or ethnicity.
03
Patients with unexplained or multiple health concerns that may be indicative of an underlying genetic disorder.
04
Individuals considering starting a family who want to assess their risk of passing on genetic conditions to their children.
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Case-finding is the process of identifying individuals who may be at risk of specific genetic conditions, while genetic testing involves analyzing DNA to detect genetic disorders, mutations, or predispositions.
Health care providers, genetic counselors, and laboratories that conduct genetic tests are typically required to file case-finding and genetic testing reports.
To fill out case-finding and genetic testing forms, one must accurately enter patient information, the reason for testing, the type of test conducted, and the results following the guidelines set by health authorities or regulatory agencies.
The purpose of case-finding and genetic testing is to identify individuals who may be at high risk for genetic disorders, promote preventive health measures, and facilitate informed medical decisions.
Information that must be reported includes patient demographics, clinical information, genetic test results, and any relevant family history of genetic conditions.
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