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Explanatory models for the cause of Fragile X Syndrome in rural Cameroon
Among the myriad causes of intellectual disability (ID), Fragile X Syndrome (FXS) is the leading genetic cause. Yet, little is known of how people affected by this condition make sense of it. The present study aimed to investigate the explanatory models for the causes of FXS in an extended family ma...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642261/ https://www.ncbi.nlm.nih.gov/pubmed/34145661 http://dx.doi.org/10.1002/jgc4.1440 |
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author | Kengne Kamga, Karen De Vries, Jantina Nguefack, Séraphin Munung, Nchangwi Syntia Wonkam, Ambroise |
author_facet | Kengne Kamga, Karen De Vries, Jantina Nguefack, Séraphin Munung, Nchangwi Syntia Wonkam, Ambroise |
author_sort | Kengne Kamga, Karen |
collection | PubMed |
description | Among the myriad causes of intellectual disability (ID), Fragile X Syndrome (FXS) is the leading genetic cause. Yet, little is known of how people affected by this condition make sense of it. The present study aimed to investigate the explanatory models for the causes of FXS in an extended family mainly affected by this condition and members of the village from which they originated in Cameroon. Using an ethnographic approach, 92 participants were interviewed (59 females and 33 males) through 10 focus group discussions and 23 in‐depth interviews between April 2018 and February 2020. Data analysis revealed four explanatory models regarding the etiologies of FXS in the community. Firstly, the curse model described a curse from the chief because of the belief that his wives did not mourn his intellectually disabled servant. Secondly, the spiritual model relates FXS to a punishment from God. Thirdly, the socioeconomic model attributes FXS to events in the prenatal and perinatal periods. Finally, the genetic model describes the pattern of inheritance of the disease in the family. This paper helps to understand the explanatory disease models that exist for FXS in rural Cameroon and could inform genetic counseling practices, community genetic education, and policymakers when drafting protocols for public engagement activities. |
format | Online Article Text |
id | pubmed-8642261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86422612022-10-14 Explanatory models for the cause of Fragile X Syndrome in rural Cameroon Kengne Kamga, Karen De Vries, Jantina Nguefack, Séraphin Munung, Nchangwi Syntia Wonkam, Ambroise J Genet Couns Original Articles Among the myriad causes of intellectual disability (ID), Fragile X Syndrome (FXS) is the leading genetic cause. Yet, little is known of how people affected by this condition make sense of it. The present study aimed to investigate the explanatory models for the causes of FXS in an extended family mainly affected by this condition and members of the village from which they originated in Cameroon. Using an ethnographic approach, 92 participants were interviewed (59 females and 33 males) through 10 focus group discussions and 23 in‐depth interviews between April 2018 and February 2020. Data analysis revealed four explanatory models regarding the etiologies of FXS in the community. Firstly, the curse model described a curse from the chief because of the belief that his wives did not mourn his intellectually disabled servant. Secondly, the spiritual model relates FXS to a punishment from God. Thirdly, the socioeconomic model attributes FXS to events in the prenatal and perinatal periods. Finally, the genetic model describes the pattern of inheritance of the disease in the family. This paper helps to understand the explanatory disease models that exist for FXS in rural Cameroon and could inform genetic counseling practices, community genetic education, and policymakers when drafting protocols for public engagement activities. John Wiley and Sons Inc. 2021-06-17 2021-12 /pmc/articles/PMC8642261/ /pubmed/34145661 http://dx.doi.org/10.1002/jgc4.1440 Text en © 2021 The Authors. Journal of Genetic Counseling published by Wiley Periodicals LLC on behalf of National Society of Genetic Counselors. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Kengne Kamga, Karen De Vries, Jantina Nguefack, Séraphin Munung, Nchangwi Syntia Wonkam, Ambroise Explanatory models for the cause of Fragile X Syndrome in rural Cameroon |
title | Explanatory models for the cause of Fragile X Syndrome in rural Cameroon |
title_full | Explanatory models for the cause of Fragile X Syndrome in rural Cameroon |
title_fullStr | Explanatory models for the cause of Fragile X Syndrome in rural Cameroon |
title_full_unstemmed | Explanatory models for the cause of Fragile X Syndrome in rural Cameroon |
title_short | Explanatory models for the cause of Fragile X Syndrome in rural Cameroon |
title_sort | explanatory models for the cause of fragile x syndrome in rural cameroon |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642261/ https://www.ncbi.nlm.nih.gov/pubmed/34145661 http://dx.doi.org/10.1002/jgc4.1440 |
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