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Systematic ReviewSystematic Review
Open Access

Advancing genetic counselling in Southern Africa

Unveiling opportunities for inclusive healthcare and genomic education for Angola

Maria Chimpolo, Shahida Moosa, Catherine Lynn T. Silao, Nasser Calumbuana, Elka Kay, Hashim Halim-Fikri, Dhavendra Kumar and Bin Alwi Zilfalil
Saudi Medical Journal April 2025, 46 (4) 335-344; DOI: https://doi.org/10.15537/smj.2025.46.4.20240370
Maria Chimpolo
From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
LLM, PhD
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Shahida Moosa
From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
MBBCh, PhD
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Catherine Lynn T. Silao
From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
MD, PhD
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Nasser Calumbuana
From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
MBBS, ABFM
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Elka Kay
From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
BSc
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Hashim Halim-Fikri
From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
BAppSc, MSc
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Dhavendra Kumar
From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
MD, DSc, PhD
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Bin Alwi Zilfalil
From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
MBBS, PhD
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Advancing genetic counselling in Southern Africa
Maria Chimpolo, Shahida Moosa, Catherine Lynn T. Silao, Nasser Calumbuana, Elka Kay, Hashim Halim-Fikri, Dhavendra Kumar, Bin Alwi Zilfalil
Saudi Medical Journal Apr 2025, 46 (4) 335-344; DOI: 10.15537/smj.2025.46.4.20240370

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Advancing genetic counselling in Southern Africa
Maria Chimpolo, Shahida Moosa, Catherine Lynn T. Silao, Nasser Calumbuana, Elka Kay, Hashim Halim-Fikri, Dhavendra Kumar, Bin Alwi Zilfalil
Saudi Medical Journal Apr 2025, 46 (4) 335-344; DOI: 10.15537/smj.2025.46.4.20240370
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  • Genetic counseling
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Saudi Medical Journal

© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

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