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LA JOLLA ENDODONTICS Baba Shoushtari, D.M.D. Practice Limited to Endodontics Patient Information: Title: (Mr., Mrs., Ms., Dr.) Date: First Name: Middle Initial: Last Name: Sex (please circle):Date
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To fill out the Li-Fraumeni Syndrome (LFS) survey by Nord, follow these steps:
02
Visit the Nord website and navigate to the LFS survey page.
03
Read the instructions and information provided about the survey and LFS.
04
Fill in your personal details such as name, age, gender, and contact information.
05
Answer the survey questions according to your knowledge and experience related to LFS.
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Submit the completed survey form.
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If you have any additional comments or information to provide, include them in the designated section.
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Wait for any further communication from Nord regarding the survey or LFS.
Who needs li-fraumeni syndrome - nord?
01
Individuals who suspect they may have Li-Fraumeni Syndrome or have been diagnosed with LFS can benefit from the resources and support provided by Nord. The organization focuses on helping families affected by rare genetic conditions and provides information about LFS, connecting patients with healthcare professionals, and facilitating research in the field. People seeking guidance, support, and assistance related to LFS can turn to Nord for help.
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What is li-fraumeni syndrome - nord?
Li-Fraumeni syndrome is a hereditary condition that increases the risk of developing several types of cancer at a young age, due to mutations in the TP53 gene.
Who is required to file li-fraumeni syndrome - nord?
Individuals who have a confirmed diagnosis of Li-Fraumeni syndrome or those with a family history of the syndrome are required to file.
How to fill out li-fraumeni syndrome - nord?
To fill out the Li-Fraumeni syndrome documentation, individuals should provide personal and family medical history, detailing any cancer diagnoses and genetic testing results if available.
What is the purpose of li-fraumeni syndrome - nord?
The purpose of Li-Fraumeni syndrome tracking is to gather data for research, improve understanding of the syndrome, inform preventative measures, and enhance patient support.
What information must be reported on li-fraumeni syndrome - nord?
Information that must be reported includes personal identification details, medical history, family history of cancer, and any genetic testing results.
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