NF + SWN Diagnosis vVARY
Children's Tumor FoundationDownload Options
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About this app
For healthcare providers managing patients who may have a diagnosis of NF or SWN
The Children’s Tumor Foundation NF + SWN Diagnosis App is designed to support healthcare providers as a useful tool for diagnosing patients who may have neurofibromatosis (NF) or schwannomatosis or a related disorder. With a special focus on the 2021 and 2022 updates to the diagnostic criteria, the app compiles the most relevant, evidence-based clinical guidelines from multiple sources into a single tool and places them at the clinician’s finger tips.
This free app was created by the Children’s Tumor Foundation as a tool for medical professionals, clinicians, genetic counselors, medical students, and general practitioners.
About Children’s Tumor Foundation:
Founded in 1978, the Children’s Tumor Foundation (CTF) began as the first grassroots organization solely dedicated to finding treatments for NF. Today, CTF is a highly recognized global nonprofit foundation, the leading force in the fight to end NF, and a model for other innovative research endeavors.
Our Mission: Drive research, expand knowledge, and advance care for the NF community.
Our Vision: End NF.
Only a medical professional can confirm a diagnosis of NF1, Legius Syndrome, or any type of schwannomatosis (including NF2-related schwannomatosis, formerly called NF2). This mobile app is a tool and not a replacement for diagnostic assessment and medical management from a healthcare provider.
This free app was created by the Children’s Tumor Foundation as a tool for medical professionals, clinicians, genetic counselors, medical students, and general practitioners.
About Children’s Tumor Foundation:
Founded in 1978, the Children’s Tumor Foundation (CTF) began as the first grassroots organization solely dedicated to finding treatments for NF. Today, CTF is a highly recognized global nonprofit foundation, the leading force in the fight to end NF, and a model for other innovative research endeavors.
Our Mission: Drive research, expand knowledge, and advance care for the NF community.
Our Vision: End NF.
Only a medical professional can confirm a diagnosis of NF1, Legius Syndrome, or any type of schwannomatosis (including NF2-related schwannomatosis, formerly called NF2). This mobile app is a tool and not a replacement for diagnostic assessment and medical management from a healthcare provider.
Version Information
- Version
- -
- Downloads
- 100+
- Updated on
- -
- Released
- Feb 23, 2023
- Requires
- Android Varies with device
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