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Diagnosis of Fragile X Syndrome: A Qualitative Study of African American Families
Authors:Jeannie Visootsak  Krista Charen  Julia Rohr  Emily Allen  Stephanie Sherman
Affiliation:1. Department of Human Genetics, Emory University, Atlanta, GA, USA
2. Department of Pediatrics, Emory University, Atlanta, GA, USA
4. 2165 N. Decatur Road, Decatur, GA, 30033, USA
3. Boston University School of Public Health, Boston, MA, USA
Abstract:Fragile X syndrome (FXS) is an inherited genetic condition with critical consequences to the proband and family members at all levels in the generations. Although evidence demonstrates that the rates of diagnosis for FXS are the same in all racial groups, age of diagnosis in African American children has been reported to occur later than in Caucasian children. Additionally, African American families are seriously under-represented in existing FXS research studies. As such, it is important to understand the possible disparities in the underlying factors to receiving a diagnosis in African American families with FXS. Herein, a qualitative approach was adopted to describe the overall FXS diagnosis experiences (pre-diagnosis, diagnosis, and post-diagnosis stages) of a convenience sample of 10 African American mothers. We identified three major findings among our participants: (1) FXS testing is not ordered immediately once a parent expresses concerns of developmental delays to the pediatricians, (2) the diagnosis is sometimes delivered in an insensitive manner with information often being outdated and unbalanced towards negative aspects, (3) communication issues among family members exists once the diagnosis is discovered. Although these qualitative data may not be representative of the whole group, these findings have significant implications for genetic counseling and our understanding in providing support and advocacy for African American families with FXS.
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