Emotional and neurocognitive deficits in fragile X
- 15 July 1994
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 51 (4) , 378-385
- https://doi.org/10.1002/ajmg.1320510416
Abstract
We have studied the neurocognitive deficit in premutation and full mutation women as compared to control women and to explore the relationship between those deficits and the incidence of emotional problems. Four groups of women were examined: two fragile X (fra(X)) negative control groups, one of which grew up in fra(X) families and one not; and two DNA positive groups, one with a premutation (CGG repeats 200). All women were assessed using the MMPI-2, the SADS-L, and a battery of neuropsychological tests. Full mutation women had lower scores on composite measures of executive function and nonverbal function. There was no difference between the groups in terms of the lifetime incidence of depressive and anxiety disorders on the SADS-L. Full mutation women displayed Lie scales higher than the other groups on the MMPI-2. Neurocognitive measures were not related to SADS-L diagnoses but were related to the Lie scale on the MMPI-2. Finally, number of CGG repeats was related to the neuropsychological variables and the Lie scale.Keywords
This publication has 26 references indexed in Scilit:
- The Neurocognitive Phenotype of Female Carriers of Fragile XJournal of Developmental & Behavioral Pediatrics, 1993
- The FMR–1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutationNature Genetics, 1993
- Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brainNature Genetics, 1993
- Problem solving limitations among cytogenetically expressing fragile X womenAmerican Journal of Medical Genetics, 1992
- Analysis of mutations at the fragile X locus using the DNA probe Ox1.9American Journal of Medical Genetics, 1992
- Detection of full fragile X mutationThe Lancet, 1992
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Absence of expression of the FMR-1 gene in fragile X syndromeCell, 1991
- Syndrome of nonverbal learning disabilities: Age differences in neuropsychological, academic, and socioemotional functioningDevelopment and Psychopathology, 1991
- Neuropsychological studies of the frontal lobes.Psychological Bulletin, 1984