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bioRxiv preprint doi: https://doi.org/10.1101/2023.01.31.526399; this version posted September 4, 2023. The copyright holder for this preprint (which was not certified by peer review) is the author/funder,

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How to fill out form alsftd-related c9orf72 hexanucleotide

01

Obtain the form for C9orf72 hexanucleotide repeat expansion testing.

02

Provide personal information such as name, date of birth, and contact details.

03

Answer medical history questions related to family history of ALS or FTD.

04

Indicate the reason for testing, explaining any symptoms or concerns.

05

If applicable, provide information about previous genetic tests related to ALS or FTD.

06

Sign and date the form to confirm consent for testing.

07

Submit the completed form to the designated testing facility or healthcare provider.

Who needs form alsftd-related c9orf72 hexanucleotide?

01

Individuals with a family history of ALS (Amyotrophic Lateral Sclerosis) or FTD (Frontotemporal Dementia).

02

Patients exhibiting symptoms related to ALS or FTD.

03

Healthcare providers seeking to confirm a diagnosis or assess genetic risk for patients.

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What is form alsftd-related c9orf72 hexanucleotide?

The form alsftd-related c9orf72 hexanucleotide refers to a genetic testing form used to screen for the C9orf72 gene mutation, which is associated with familial forms of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS).

Who is required to file form alsftd-related c9orf72 hexanucleotide?

Individuals who are suspected of having a genetic predisposition to ALS or FTD, particularly those with a family history of these conditions, are typically required to file this form.

How to fill out form alsftd-related c9orf72 hexanucleotide?

To fill out the form, individuals must provide personal and family medical history, specific details about symptoms, and consent for genetic testing. It is important to follow the instructions provided with the form and seek assistance from a healthcare professional if needed.

What is the purpose of form alsftd-related c9orf72 hexanucleotide?

The purpose of the form is to facilitate genetic testing for the C9orf72 hexanucleotide repeat expansion, helping to diagnose individuals with ALS or FTD and allowing for better understanding and management of the conditions.

What information must be reported on form alsftd-related c9orf72 hexanucleotide?

The information required typically includes personal identification details, family history of neurodegenerative diseases, clinical symptoms experienced by the individual, and consent for genetic testing and disclosure of results.

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