Article
[Fragile X syndrome and mental retardation].
Revista de neurologia - 1 Jul 1997
Estévez-González A, Roig C, Piles S, Pineda M, García-Sánchez C
Abstract excerpt
INTRODUCTION: Fragile-X syndrome is characterized by the presence of a fragile site (gap) on Xq 27.3 and the transcriptional inhibition of a mRNA protein-binding gene called FMR-1. Neuropsychological features include cognitive impairment, attention deficit disorder with and without hyperactivity,...
Topics
- Adult
- Chromosome Aberrations
- Chromosome Disorders
- Female
- Fragile X Syndrome
- Humans
- Intellectual Disability
- Male
- Phenotype
