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PMID: 12853198 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH.

Lancet (London, England) ·Vol. 362 ·No. 9377 ·2003-07-05 ·Pages 39-41

Sampson JR, Dolwani S, Jones S, Eccles D, Ellis A, Evans DG, Frayling I, Jordan S, Maher ER, Mak T, Maynard J, Pigatto F, Shaw J, Cheadle JP

Abstract

Familial adenomatous polyposis (FAP) and attenuated FAP are autosomal dominant disorders characterised by multiple colorectal adenomas and cancers. Both are caused by inherited mutations in the APC gene, and management includes genetic testing, colonoscopic surveillance, and prophylactic surgery for the relatives of index cases. Among 614 families recorded in six regional registers of polyposis in the UK, we identified 111 with neither dominant transmission nor evidence of APC mutation. Molecular genetic analysis showed that 25 had biallelic mutations of the MYH gene. Since our data show that MYH polyposis can be transmitted as an autosomal recessive trait, a change in genetic counselling, testing, and surveillance is needed.

MeSH Terms
Adenomatous Polyposis Coli/epidemiology,genetics Adolescent Adult Aged DNA Glycosylases Female Genes, Recessive Humans Male Middle Aged Molecular Sequence Data Mutation N-Glycosyl Hydrolases/genetics Registries United Kingdom/epidemiology
Chemicals
DNA Glycosylases N-Glycosyl Hydrolases mutY adenine glycosylase
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Sampson Julian R
Institute of Medical Genetics, University of Wales College of Medicine, Heath Park, Cardiff, UK. sampson@cardiff.ac.uk
Dolwani Sunil
Jones Sian
Eccles Diana
Ellis Anthony
Evans D Gareth
Frayling Ian
Jordan Sheila
Maher Eamonn R
Mak Tony
Maynard Julie
Pigatto Francesca
Shaw Joan
Cheadle Jeremy P
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
1474-547X
Published
2003-07-05
Pages
39-41
Language
English
Region
England
NLM ID
2985213R
Subset
IM
Databases
RefSeq
NM_012222
Corrections
CommentIn
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