Myh-associated Polyposis
What's New
Last Posted: Jan 04, 2024
- Secondary (additional) findings from the 100,000 Genomes Project: disease manifestation, healthcare outcomes and costs of disclosure.
Joshua Nolan et al. Genet Med 2023 101051 - Secondary (additional) findings from the 100,000 Genomes Project: disease manifestation, healthcare outcomes and costs of disclosure
J Nolan et al, Genetics in Medicine, December 19, 2023 - Identifying mutations for MYH-associated polyposis.
Prior Thomas W, et al. Current protocols in human genetics 2010 0 Unit 10.13 - CLINGEN Actionability Report for MUTYH-Associated Polyposis - MUTYH
ClinGen Actionability Working Group - Lower gastrointestinal neuroendocrine neoplasms associated with hereditary cancer syndromes: a case series.
Kidambi Trilokesh D et al. Familial cancer 2017 Oct 16(4) 537-543 - ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).
- The first mutations in the MYH gene reported in Moroccan colon cancer patients.
Laarabi F Z, et al. Gene 2012 3 (1) 55-8 - MYH-associated polyposis
From NCATS Genetic and Rare Diseases Information Center - Prevalence of MYH-associated polyposis related to three recurrent mutations in Morocco.
Laarabi F Z, et al. Annals of human biology 2011 5 (3) 360-3 - APC, MYH, and the correlation genotype-phenotype in colorectal polyposis.
Lefevre Jérémie H, et al. Annals of surgical oncology 2009 4 (4) 871-7
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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