BRCA mutations in a cohort of Iraqi patients presenting to a tertiary referral center

dc.contributor.authorFarra, Chantal G.
dc.contributor.authorDagher, Christelle
dc.contributor.authorHamadeh, Lama N.
dc.contributor.authorEl-Saghir, Nagi S.
dc.contributor.authorMukherji, Deborah M.
dc.contributor.departmentPathology and Laboratory Medicine
dc.contributor.departmentInternal Medicine
dc.contributor.departmentMedical Genetics
dc.contributor.departmentDivision of Hematology Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:10:01Z
dc.date.available2025-01-24T12:10:01Z
dc.date.issued2019
dc.description.abstractBACKGROUND: Unique pathogenic mutations in BRCA1 and 2 genes have been reported in different populations of patients originating from the Middle East region. Limited data are available for the Iraqi population. For many reasons a large number of Iraqi patients present to Lebanon for medical care. This is the first report of BRCA full gene sequencing conducted in a cohort of high-risk patients originating from Iraq. METHODS: This is a retrospective review of Iraqi patients diagnosed with breast or ovarian cancer referred for BRCA mutation testing at the American University of Beirut from January 2012 to October 2018. RESULTS: Of the 42 Iraqi women who underwent genetic testing at our institution, 3 BRCA pathogenic variants were found. Two mutations in BRCA1 c.224_227delAAAG and c.5431C > T and one mutation in BRCA2 c.5576_5579delTTAA were identified. Three other patients had sequence changes considered as variants of undetermined significance. CONCLUSION: In this cohort of high-risk patients, one out of the three pathogenic BRCA variants detected has not previously been reported in the Middle Eastern population. Further studies are required to delineate the spectrum of BRCA mutations in the Iraqi population.
dc.identifier.doihttps://doi.org/10.1186/s12881-019-0885-9
dc.identifier.eid2-s2.0-85071760276
dc.identifier.pmid31488070
dc.identifier.urihttp://hdl.handle.net/10938/32228
dc.language.isoen
dc.publisherNLM (Medline)
dc.relation.ispartofBMC medical genetics
dc.sourceScopus
dc.subjectBrca1
dc.subjectBrca2
dc.subjectBreast cancer
dc.subjectIraq
dc.subjectMiddle east
dc.subjectAdult
dc.subjectAged
dc.subjectBrca1 protein
dc.subjectBrca2 protein
dc.subjectBreast neoplasms
dc.subjectCohort studies
dc.subjectFemale
dc.subjectGenes, brca2
dc.subjectGenetic predisposition to disease
dc.subjectHumans
dc.subjectMiddle aged
dc.subjectMutation
dc.subjectOvarian neoplasms
dc.subjectRetrospective studies
dc.subjectTertiary care centers
dc.subjectBrca1 protein, human
dc.subjectBrca2 protein, human
dc.subjectBreast tumor
dc.subjectCohort analysis
dc.subjectGenetic predisposition
dc.subjectGenetics
dc.subjectHuman
dc.subjectOvary tumor
dc.subjectRetrospective study
dc.subjectTertiary care center
dc.subjectTumor suppressor gene
dc.titleBRCA mutations in a cohort of Iraqi patients presenting to a tertiary referral center
dc.typeArticle

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