Search: onr:"swepub:oai:lup.lub.lu.se:c5daada8-9860-4b25-816a-1bce4a5fbf83" >
Expanding the genot...
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Rohlin, AnnaGothenburg University,Göteborgs universitet,University of Gothenburg,Institutionen för biomedicin,Institute of Biomedicine
(author)
Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing
- Article/chapterEnglish2017
Publisher, publication year, extent ...
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2016-09-30
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Springer Science and Business Media LLC,2017
Numbers
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LIBRIS-ID:oai:lup.lub.lu.se:c5daada8-9860-4b25-816a-1bce4a5fbf83
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https://lup.lub.lu.se/record/c5daada8-9860-4b25-816a-1bce4a5fbf83URI
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https://doi.org/10.1007/s10689-016-9934-0DOI
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http://kipublications.ki.se/Default.aspx?queryparsed=id:135625466URI
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https://gup.ub.gu.se/publication/246627URI
Supplementary language notes
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Language:English
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Summary in:English
Part of subdatabase
Classification
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Subject category:art swepub-publicationtype
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Subject category:ref swepub-contenttype
Notes
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Hereditary syndromes causing colorectal cancer include both polyposis and non-polyposis syndromes. Overlapping phenotypes between the syndromes have been recognized and this make targeted molecular testing for single genes less favorable, instead there is a gaining interest for multi-gene panel-based approaches detecting both SNVs, indels and CNVs in the same assay. We applied a panel including 19 CRC susceptibility genes to 91 individuals of six phenotypic subgroups. Targeted NGS-based sequencing of the whole gene regions including introns of the 19 genes was used. The individuals had a family history of CRC or had a phenotype consistent with a known CRC syndrome. The purpose of the study was to demonstrate the diagnostic difficulties linked to genotype-phenotype diversity and the benefits of using a gene panel. Pathogenicity classification was carried out on 46 detected variants. In total we detected sixteen pathogenic or likely pathogenic variants and 30 variants of unknown clinical significance. Four of the pathogenic or likely pathogenic variants were found in BMPR1A in patients with unexplained familial adenomatous polyposis or atypical adenomatous polyposis, which extends the genotype-phenotype spectrum for this gene. Nine patients had more than one variant remaining after the filtration, including three with truncating mutations in BMPR1A, PMS2 and AXIN2. CNVs were found in three patients, in upstream regions of SMAD4, MSH3 and CTNNB1, and one additional individual harbored a 24.2 kb duplication in CDH1 intron1.
Subject headings and genre
Added entries (persons, corporate bodies, meetings, titles ...)
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Rambech, EvaLund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine(Swepub:lu)onk-era
(author)
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Kvist, AndersLund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine(Swepub:lu)ekol-akv
(author)
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Törngren, ThereseLund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine(Swepub:lu)onk-tsa
(author)
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Eiengård, FridaGothenburg University,Göteborgs universitet,University of Gothenburg,Institutionen för biomedicin,Institute of Biomedicine
(author)
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Lundstam, UlfGothenburg University,Göteborgs universitet,University of Gothenburg,Institutionen för kliniska vetenskaper, Avdelningen för kirurgi,Institute of Clinical Sciences, Department of Surgery
(author)
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Zagoras, TheofanisGothenburg University,Göteborgs universitet,University of Gothenburg,Institutionen för biomedicin,Institute of Biomedicine
(author)
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Gebre-Medhin, SamuelLund University,Lunds universitet,Avdelningen för klinisk genetik,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Clinical Genetics,Department of Laboratory Medicine,Faculty of Medicine(Swepub:lu)mphy-sgm
(author)
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Borg, ÅkeLund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine(Swepub:lu)onk-abo
(author)
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Björk, JanKarolinska Institute
(author)
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Nilbert, MefLund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,University of Copenhagen(Swepub:lu)onk-mni
(author)
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Nordling, MargaretaUniversity of Gothenburg
(author)
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University of GothenburgInstitutionen för biomedicin
(creator_code:org_t)
Related titles
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In:Familial Cancer: Springer Science and Business Media LLC16:2, s. 195-2031389-96001573-7292
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Rohlin, Anna
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Rambech, Eva
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Kvist, Anders
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Törngren, Theres ...
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Eiengård, Frida
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Lundstam, Ulf
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Zagoras, Theofan ...
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Gebre-Medhin, Sa ...
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Borg, Åke
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Björk, Jan
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Nilbert, Mef
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Nordling, Margar ...
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- About the subject
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- MEDICAL AND HEALTH SCIENCES
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MEDICAL AND HEAL ...
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and Basic Medicine
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and Medical Genetics
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- MEDICAL AND HEALTH SCIENCES
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MEDICAL AND HEAL ...
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and Clinical Medicin ...
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and Cancer and Oncol ...
- Articles in the publication
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Familial Cancer
- By the university
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Lund University
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Karolinska Institutet
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University of Gothenburg