Literature DB >> 8844074

Neuropsychological profiles of three sisters homozygous for the fragile X premutation.

M M Mazzocco1, J J Holden.   

Abstract

Fragile X syndrome (fraX) is associated with an amplification of a CGG repeat within the fraX mental retardation (FMR-1) gene. We describe an exceptional family in which 3 adult sisters are homozygous for the FMR-1 premutation. Each sister inherited 2 premutation alleles (ca. 80 CGG repeats) from their biologically unrelated parents. The 3 sisters were administered measures of executive function, visual spatial, memory, and verbal skills. Deficiencies in the first 2 of these domains have been reported among females with the full mutation. The sisters' performances were compared with available normative data and with published group means for females affected by fraX. These women did not appear to have verbal or memory difficulties. None of the women demonstrated a global executive function deficit, and none had global deficits in spatial ability. The profiles of these sisters are consistent with reports that the fragile X premutation does not affect cognitive performance.

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Year:  1996        PMID: 8844074     DOI: 10.1002/(SICI)1096-8628(19960809)64:2<323::AID-AJMG18>3.0.CO;2-H

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 in total

1.  Clinical phenotypes of a juvenile sibling pair carrying the fragile X premutation.

Authors:  Kirin Basuta; Vivien Narcisa; Alyssa Chavez; Madhur Kumar; Louise Gane; Randi Hagerman; Flora Tassone
Journal:  Am J Med Genet A       Date:  2011-02-22       Impact factor: 2.802

2.  Wild-type male offspring of fmr-1+/- mothers exhibit characteristics of the fragile X phenotype.

Authors:  Bojana Zupan; Miklos Toth
Journal:  Neuropsychopharmacology       Date:  2008-01-02       Impact factor: 7.853

3.  Carriage of One or Two FMR1 Premutation Alleles Seems to Have No Effect on Illness Severity in a FXTAS Female with an Autozygous FMR1 Premutation Allele.

Authors:  Laia Rodriguez-Revenga; Javier Pagonabarraga; Beatriz Gómez-Anson; Olga López-Mourelo; Silvia Izquierdo; Maria Isabel Alvarez-Mora; Esther Granell; Irene Madrigal; Montserrat Milà
Journal:  Cerebellum       Date:  2016-10       Impact factor: 3.847

4.  A family with two female siblings with compound heterozygous FMR1 premutation alleles.

Authors:  K Basuta; R Lozano; A Schneider; C M Yrigollen; D Hessl; R J Hagerman; F Tassone
Journal:  Clin Genet       Date:  2013-07-28       Impact factor: 4.438

5.  Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed.

Authors:  Ling M Wong; Naomi J Goodrich-Hunsaker; Yingratana McLennan; Flora Tassone; Danielle Harvey; Susan M Rivera; Tony J Simon
Journal:  J Neurodev Disord       Date:  2012-11-13       Impact factor: 4.025

  5 in total

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