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Bio
Helen became part of the rare disease community in 2004 when she lost her first child, Madeleine, to Trisomy 18 (Edwards Syndrome), and soon after established a contact point for families in South Africa affected by the condition. As a result of her personal experience and keen to make a difference, Helen completed a PhD at the University of KwaZulu Natal (UKZN) in 2017 investigating the renewed need for the care and prevention of congenital disorders in South Africa. She continued her research work as a post-doctoral fellow for four years at UKZN and a year at the University of Pretoria, and in January 2023 was appointed as Extraordinary Associate Professor at the Center for Metabolomics, North-West University. Simultaneous to her research work, Helen has been continually involved as a patient advocate, initially leading Genetic Alliance South Africa NPO (2014-2019) and as a Director of Rare Diseases South Africa (RDSA) since April 2019, overseeing Research and Epidemiology.
Research Interests
Papers共 36 篇Author StatisticsCo-AuthorSimilar Experts
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Research Square (Research Square) (2023)
Journal of community geneticsno. 3 (2023): 241-262
Research Square (Research Square) (2023)
Aminkeng Zawuo Leke,Helen Malherbe,Emma Kalk,Ushma Mehta, Phylis Kisa,Lorenzo D Botto, Idowu Ayede,Lee Fairlie,Nkwati Michel Maboh,Ieda Orioli,Rebecca Zash,Ronald Kusolo,
PLOS global public healthno. 6 (2023)
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskundeno. 12 (2023): 9-9
Annals of Global Healthno. 1 (2023): 6-6
Research Square (Research Square) (2023)
PAMJ Clinical Medicine (2022)
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