Literature DB >> 12476071

Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis.

Danuta Z Loesch1, Richard M Huggins, Quang M Bui, Jennifer L Epstein, Annette K Taylor, Randi Jensen Hagerman.   

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.

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Year:  2002        PMID: 12476071     DOI: 10.1097/00004703-200212000-00004

Source DB:  PubMed          Journal:  J Dev Behav Pediatr        ISSN: 0196-206X            Impact factor:   2.225


  29 in total

Review 1.  The state of synapses in fragile X syndrome.

Authors:  Brad E Pfeiffer; Kimberly M Huber
Journal:  Neuroscientist       Date:  2009-03-26       Impact factor: 7.519

2.  Longitudinal profiles of expressive vocabulary, syntax and pragmatic language in boys with fragile X syndrome or Down syndrome.

Authors:  Gary E Martin; Molly Losh; Bruno Estigarribia; John Sideris; Joanne Roberts
Journal:  Int J Lang Commun Disord       Date:  2013-04-19       Impact factor: 3.020

3.  FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 alleles.

Authors:  David E Godler; Howard R Slater; Quang M Bui; Michele Ono; Freya Gehling; David Francis; David J Amor; John L Hopper; Randi Hagerman; Danuta Z Loesch
Journal:  J Mol Diagn       Date:  2011-06-30       Impact factor: 5.568

4.  A Multimethod Analysis of Pragmatic Skills in Children and Adolescents With Fragile X Syndrome, Autism Spectrum Disorder, and Down Syndrome.

Authors:  Gary E Martin; Lauren Bush; Jessica Klusek; Shivani Patel; Molly Losh
Journal:  J Speech Lang Hear Res       Date:  2018-12-10       Impact factor: 2.297

5.  Perseveration in the connected speech of boys with Fragile X syndrome with and without autism spectrum disorder.

Authors:  Gary E Martin; Joanne E Roberts; Nancy Helm-Estabrooks; John Sideris; Jacqueline Vanderbilt; Lauren Moskowitz
Journal:  Am J Intellect Dev Disabil       Date:  2012-09

6.  Autism spectrum phenotype in males and females with fragile X full mutation and premutation.

Authors:  Sally Clifford; Cheryl Dissanayake; Quang M Bui; Richard Huggins; Annette K Taylor; Danuta Z Loesch
Journal:  J Autism Dev Disord       Date:  2007-04

7.  Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice.

Authors:  Adam J Iliff; Abigail J Renoux; Amy Krans; Karen Usdin; Michael A Sutton; Peter K Todd
Journal:  Hum Mol Genet       Date:  2012-12-18       Impact factor: 6.150

8.  Teasing apart the heterogeneity of autism: Same behavior, different brains in toddlers with fragile X syndrome and autism.

Authors:  Heather Cody Hazlett; Michele D Poe; Amy A Lightbody; Guido Gerig; James R Macfall; Allison K Ross; James Provenzale; Arianna Martin; Allan L Reiss; Joseph Piven
Journal:  J Neurodev Disord       Date:  2009-03       Impact factor: 4.025

Review 9.  Review of targeted treatments in fragile X syndrome.

Authors:  Andrew Ligsay; Randi J Hagerman
Journal:  Intractable Rare Dis Res       Date:  2016-08

10.  Psychosis and catatonia in fragile X: Case report and literature review.

Authors:  Tri Indah Winarni; Andrea Schneider; Neera Ghaziuddin; Andreea Seritan; Randi J Hagerman
Journal:  Intractable Rare Dis Res       Date:  2015-08
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