
This book tells how Ricaurte is a genetic cluster of Fragile X syndrome (FXS) with the highest prevalence in the world through a research project co-funded by the Universidad del Valle and the MIND Institute of the University of California at Davis. SXF is described in depth, from genomics, through the genotype and phenotype of SXF to treatment in experimentation. In addition, the characteristics of Ricaurte, a township in the municipality of Bolivar in Valle del Cauca, are shown, including its foundation, social contextualization, its regional visualization marked by a religious and national context by the book El Divino by the writer Gustavo Alvarez Gardeazabal, which describes the intellectual disability of a significant number of its inhabitants who are masterfully described in that book. It also describes the project “Population medical genetics in a Colombian township with high prevalence of Fragile X syndrome”, which was an ambitious proposal, which in addition to establishing the prevalence of allelic variants gray zone, permutation and complete mutation of the FMR1 gene and its comparison with the accepted global prevalence, a public health intervention with genetic and reproductive counseling to those who could have children affected by FXS or suffer from associated diseases, such as FXTAS or FXPOI, was achieved. With the methodology of reaching the homes and all the inhabitants, requesting informed consent, taking blood samples, delivering results, establishing inter-family relationships through specialized software and doing genetic and reproductive counseling, it shows how the researchers were integrated with the community on a daily basis and understood the reality of the country in poor families with several members with intellectual disabilities or the fears of those who might have affected children; It was possible to demonstrate that Ricaurte is a genetic conglomerate of SXF with the highest prevalence in the world, where there is the family with the highest number of affected members reported in the literature and where an intervention was made that will impact with the decrease in the number of new cases in order to prevent the perpetuation of the genetic and secondary social problem.
CONTENTS
REFLECTION
FOREWORD
CHAPTER 1 FRAGILE X SYNDROME
Wilmar Saldarriaga Gil, Jase Vicente Forero Forero,
Laura Yuriko González Teshima, Carlos A. Fandino Losada,
Carolina Isaza de Lourido, Randi f. Hagerman
CHAPTER 2
TREATMENT IN FRAGILE X SYNDROME
Randi f. Hagerman, Wilmar Saldarriaga Gil
CHAPTER 3
RICAURTE
Wilmar Saldarriaga Gil, Jase Vicente Forero Forero, Laura Yuriko González Teshima,
Carlos Andrés Fandiño Losada, Carolina Isaza de Lourido
CHAPTER 4
POPULATION MEDICAL GENETICS AND GENETIC CLUSTERS
Wilmar Saldarriaga Gil,
Jase Vicente Forero Forero, Carlos Andrés Fandiño Losada, Carolina Isaza Lourido.
CHAPTER 5
PREVALENCE OF THE ALLELIC VARIANTS GRAY ZONE, PREMUTATION AND COMPLETE MUTATION OF THE FMR1 GENE IN INHABITANTS OF RICAURTE
Wilmar Saldarriaga Gil, Jose Vicente Forero Forero,
Laura Yuriko González Teshima, José Rafael Tovar,
Carolina Isaza de Lourido, Marisol Silva,
Flora Tassone, Sergio Aguilar Gaxiola,
Randi f. Hagerman, Carlos Andrés Fandiño Losada
CHAPTER 6
GENEALOGIES OF FAMILIES WITH FRAGILE X SYNDROME IN RICAURTE
Jose Vicente Forero Forero,
Laura Yuriko González Teshima,
Wilmar Saldarriaga Gil
CHAPTER 7
GENETIC, MEDICAL AND REPRODUCTIVE COUNSELING IN WOMEN WITH COMPLETE MUTATION AND CARRIERS OF THE PREMUTATION OF FRAGILE X SYNDROME IN A GENETIC CONGLOMERATE
Wilmar Saldarriaga Gil, Jose Vicente Forero Forero,
Laura Yuriko González Teshima, Julian Ramírez Cheyne,
Especificaciones por formato:
ISBN-13: 9789587659184
DOI: 10.25100/peu.149
Idioma del texto: Inglés
Número de edición: 1
País de publicación: Colombia
Año de publicación: 2018
Número absoluto de páginas: 148 páginas
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