Effect of the Deficits of Fragile X Mental Retardation Protein on Cognitive Status of Fragile X Males and Females Assessed by Robust Pedigree Analysis
- 1 December 2002
- journal article
- research article
- Published by Wolters Kluwer Health in Journal of Developmental & Behavioral Pediatrics
- Vol. 23 (6) , 416-423
- https://doi.org/10.1097/00004703-200212000-00004
Abstract
The effect of the fragile X mental retardation 1 (FMR1) gene product (fragile X mental retardation protein [FMRP]) deficits on Full-Scale IQ (FSIQ) and FSIQ-adjusted Wechsler subtests and index scores in fragile X disorder were assessed using a robust modification of the maximum likelihood estimators for pedigree data. The results from 144 extended families have demonstrated a linear effect of progressively reduced levels of FMRP on the FSIQ and all subtest and summary scores in either gender. The effect of FMRP in decreasing FSIQ-adjusted subtest scores was highly significant for Digit Span, Symbol Search, Object Assembly, and Picture Arrangement, with a consistent trend in both genders. Heritability for FSIQ and unadjusted subtest scores estimated from the covariance model did not exceed 50% and varied widely from the highest for Verbal score to the lowest for Picture Completion score. Possible mechanisms by which FMRP deficit impacts on specific weaknesses in fragile X are considered on the basis of present data.Keywords
This publication has 38 references indexed in Scilit:
- Profile of cognitive functioning in women with the fragile X mutation.Neuropsychology, 2001
- Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats.Journal of Medical Genetics, 1998
- Phenotypic Involvement in Females With the FMR1 Gene MutationAmerican Journal on Mental Retardation, 1997
- Molecular-clinical correlations in males with an expanded FMR1 mutationAmerican Journal of Medical Genetics, 1996
- Contribution of the FMR1 gene mutation to human intellectual dysfunctionNature Genetics, 1995
- High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR‐1 mutation associated with protein expressionAmerican Journal of Medical Genetics, 1994
- Molecular‐neurobehavioral associations in females with the fragile X full mutationAmerican Journal of Medical Genetics, 1994
- Absence of expression of the FMR-1 gene in fragile X syndromeCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Neuropsychological dimensions of the fragile X syndrome: Support for a non-dominant hemisphere dysfunction hypothesisNeuropsychologia, 1990