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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Rare Diseases
Last data update: Apr 18, 2024
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Li-fraumeni Syndrome[original query]>>Evidence Synthesis [Product Type]
Cancer surveillance for patients with Li-Fraumeni Syndrome in Brazil: A cost-effectiveness analysis.
Isadora A Frankenthal et al. Lancet regional health. Americas 2023 12100265
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Population-Based Newborn Screening for Germline TP53 Variants: Clinical Benefits, Cost-Effectiveness, and Value of Further Research.
Kunst Natalia et al. Journal of the National Cancer Institute 2022
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CLINGEN Actionability Report for Li-Fraumeni Syndrome - TP53
ClinGen Actionability Working Group
CLINGEN Actionability Report for Retinoblastoma-RB1
ClinGen Actionability Working Group
Cost-effectiveness of early cancer surveillance for patients with Li-Fraumeni syndrome.
Tak Casey R et al. Pediatric blood & cancer 2019 Feb e27629
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Families' and health care professionals' attitudes towards Li-Fraumeni Syndrome testing in children: a systematic review.
Warby Meera et al. Clinical genetics 2018 Sep
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A Systematic Review of How Young People Live with Inherited Disease: What Can We Learn for Li-Fraumeni Syndrome?
Forbes Shepherd Rowan et al. Journal of adolescent and young adult oncology 2018 Jul
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Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis
Ballinger Mandy L et al. JAMA oncology 2017 Aug
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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