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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, PhDShahida 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, PhDCatherine 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, PhDNasser 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, ABFMElka 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.
BScHashim 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, MScDhavendra 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, PhDBin 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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In this issue
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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