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West Midlands Familial Hypercholesterolaemia Service (WMFHS) Referral Form Patient\'s Surname: Previous Surname (If known): Forenames: D.O.B:Age: NHS No: Address:Postcode: Telephone No. Daytime: Mobile:
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How to fill out fh genetic screening referral

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How to fill out fh genetic screening referral

01
Obtain a referral from a healthcare provider.
02
Contact a genetic counselor or specialist to schedule an appointment.
03
Provide a detailed medical history to the genetic counselor.
04
Provide a blood sample for genetic testing.
05
Attend follow-up appointments as needed to discuss results and next steps.

Who needs fh genetic screening referral?

01
Individuals with a family history of familial hypercholesterolemia (fh) or high cholesterol levels.
02
Individuals who have experienced early cardiovascular events or have a history of premature heart disease.
03
Individuals with genetic conditions or syndromes that are known to be associated with fh.

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FH genetic screening referral is a process where individuals can be tested for inherited genetic conditions that may predispose them to familial hypercholesterolemia.
Healthcare providers or genetic counselors may be required to file fh genetic screening referral for their patients.
To fill out fh genetic screening referral, healthcare providers need to collect information about the patient's medical history, family history, and any potential genetic conditions.
The purpose of fh genetic screening referral is to identify individuals who may be at risk for familial hypercholesterolemia and provide appropriate interventions or treatments.
The information reported on fh genetic screening referral may include the patient's personal information, medical history, family history of genetic disorders, and any genetic testing results.
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