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Fragile X Syndrome

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Figure

Tabla 1. Comparison of the expansion risk from premutation to full mutation (FM) between reported percentages depending solely in the number of  CGG repeats 2  and recently reported percentages depending in AGG interruptions and maternal 30
Tabla 2. Clinical characteristics of patients with full mutation and Fragile X Syndrome 2,21
Figure 1. Description of the typical phenotypic characteristics of Fragile X  Syndrome.
Figure 3. Therapeutic targets and FXS physiopathogenesis. In a neuron with a  normal range of CGG repeats in the FMR1 gene, there is a euchromatin structural  conformation which allows the entry of transcription machinery, due to the  acetylation of histon

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