Assessment of genetic counselling and testing of patients diagnosed with invasive breast carcinoma in two South African breast units

dc.contributor.authorMukendi, Ilunga Valerien
dc.contributor.supervisorCubasch, H.
dc.contributor.supervisorNietz, S.
dc.contributor.supervisorBianca, R.
dc.date.accessioned2024-11-11T13:00:47Z
dc.date.available2024-11-11T13:00:47Z
dc.date.issued2023
dc.descriptionA research report submitted in partial fulfillment of the requirements for the degree of Master of Medicine to the Faculty of Health Sciences, School of Medicine, University of the Witwatersrand, Johannesburg, 2023
dc.description.abstractGenetic counselling and testing can be helpful and enable further management when a carrier is identified early. Mutations in BRCA 1/2 situated on chromosomes 17q21 and 13q12-13 are rare. BRCA 1/2 are tumour suppressor genes essential for preserving genomic integrity, and their mutations will lead to DNA repair deficiency and persistent impaired DNA replication. As a result, dysplasia and breast malignancy will occur. This study was conducted at Charlotte Maxexe Johannesburg Academic Hospital, the breast unit at Chris Hani Baragwanath Academic Hospital, the Division of Human Genetics at the National Health Laboratory Service and the University of the Witwatersrand. A total of 498 patients with breast cancer participated in the study. The study population was predominantly black (n=437; 87.75%), with 61 (12.25%) white patients. Most patients were in the 51-60 age group (n=134; 26.91%). There were 80 (16.06%) patients with a known family history of breast/ovarian cancer. Most patients (282; 56.63%) were not eligible for genetic counselling and testing. Of the 216 (43.37%) eligible patients, 39 (18.06%) received genetic counselling, 176 (81.4%) did not, and one (0.46%) refused counselling. All counselled patients received next-generation sequencing testing. Our findings show that next-generation sequencing is still underused in our health institutions. Most patients were not offered counselling despite meeting the criteria
dc.description.submitterMM20245
dc.facultyFaculty of Health Sciences
dc.identifierhttps://orcid.org/ 0000-0002-3458-1187
dc.identifier.citationMukendi, Ilunga Valerien. (2024). Assessment of genetic counselling and testing of patients diagnosed with invasive breast carcinoma in two South African breast units [Master’s dissertation, University of the Witwatersrand, Johannesburg]. WireDSpace..https://hdl.handle.net/10539/42340
dc.identifier.urihttps://hdl.handle.net/10539/42340
dc.language.isoen
dc.publisherUniversity of the Witwatersrand, Johannesburg
dc.rights© 2023 University of the Witwatersrand, Johannesburg. All rights reserved. The copyright in this work vests in the University of the Witwatersrand, Johannesburg. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of University of the Witwatersrand, Johannesburg.
dc.rights.holderUniversity of the Witwatersrand, Johannesburg
dc.schoolSchool of Clinical Medicine
dc.subjectGenetic testing
dc.subjectInvasive breast cancer
dc.subjectBRCA
dc.subjectUCTD
dc.subject.otherSDG-3: Good health and well-being
dc.titleAssessment of genetic counselling and testing of patients diagnosed with invasive breast carcinoma in two South African breast units
dc.typeDissertation
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