[Fragile X chromosomes and fragile X syndrome]
Susanne Eriksen Boonen1, Karen Grønskov, Karen Brøndum-Nielsen
1Kennedy Instituttet-Statens Øjenklinik, Glostrup.
Abstract:
A case story is presented of a child diagnosed by chromosome analysis to be carrier of the fragile X chromosome at a low frequency in cultured lymphocytes. DNA analysis of the FMR1 gene at a later date did not reveal expansion of the FMR1 repeat, thereby refuting the diagnosis of fragile X syndrome. The discrepancy was discovered only when years later other family members came for counselling due to subsequent development of DNA-based analyses. It is recommended that persons and families investigated before DNA methods were used are re-evaluated and re-examined when relevant. Genetic diagnoses need regular revision, and information to families is important.
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