Literature DB >> 3337608

Psychiatric disability in female carriers of the fragile X chromosome.

A L Reiss1, R J Hagerman, S Vinogradov, M Abrams, R J King.   

Abstract

Fragile X syndrome, an X-linked genetic condition, is an important genetic cause of mental retardation in males. In addition to mental retardation, hemizygous males with fragile X syndrome appear to have a greater likelihood of displaying behaviors classified under the diagnostic category of pervasive developmental disorder than would be expected on the basis of mental retardation alone. Although the majority of female heterozygotes with the fragile X genetic defect are of normal intelligence, our clinical work with this population and a recent case report have suggested that females with fragile X syndrome have an increased rate of schizophrenia spectrum and affective disorders. In this study, the relationship of the fragile X genetic defect to psychopathology in female heterozygotes is investigated by psychiatric evaluation of 35 obligate female carriers of the fragile X chromosome and a comparison group of 24 fragile X-negative controls. Female fragile X carriers were found to have a greater frequency of psychopathology associated with schizophrenia spectrum diagnoses, particularly schizotypal features. A weaker association between the fragile X genetic defect and chronic affective disorders was detected. The specificity of the neuropsychiatric phenotype occurring in particular genetic conditions such as the fragile X syndrome adds a potentially valuable tool to the study of psychopathology in the general population.

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Year:  1988        PMID: 3337608     DOI: 10.1001/archpsyc.1988.01800250029005

Source DB:  PubMed          Journal:  Arch Gen Psychiatry        ISSN: 0003-990X


  18 in total

1.  Parental inheritance and psychological disability in fragile X females.

Authors:  A L Reiss; L Freund; S Vinogradov; R Hagerman; A Cronister
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

2.  Sex-specific rates of transmission of psychosis in the New England high-risk family study.

Authors:  Jill M Goldstein; Sara Cherkerzian; Larry J Seidman; Tracey L Petryshen; Garrett Fitzmaurice; Ming T Tsuang; Stephen L Buka
Journal:  Schizophr Res       Date:  2011-02-18       Impact factor: 4.939

Review 3.  The assessment of schizotypy and its clinical relevance.

Authors:  Oliver J Mason
Journal:  Schizophr Bull       Date:  2015-03       Impact factor: 9.306

4.  Genetic Counseling for Fragile X Syndrome: Recommendations of the National Society of Genetic Counselors.

Authors:  N McIntosh; L W Gane; A McConkie-Rosell; R L Bennett
Journal:  J Genet Couns       Date:  2000-08       Impact factor: 2.537

5.  X chromosome imprinting in fragile X syndrome.

Authors:  W D Yu; S L Wenger; M W Steele
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

Review 6.  Fragile X-associated disorders: a clinical overview.

Authors:  Anne Gallagher; Brian Hallahan
Journal:  J Neurol       Date:  2011-07-12       Impact factor: 4.849

Review 7.  Fragile X syndrome.

Authors:  E Wiebe; A Wiebe
Journal:  Can Fam Physician       Date:  1994-02       Impact factor: 3.275

8.  Social cognition skills among females with fragile X.

Authors:  M M Mazzocco; B F Pennington; R J Hagerman
Journal:  J Autism Dev Disord       Date:  1994-08

9.  Neurobehavioral effects of the fragile X premutation in adult women: a controlled study.

Authors:  A L Reiss; L Freund; M T Abrams; C Boehm; H Kazazian
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

10.  Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?

Authors:  M Zatz; H Vallada; M S Melo; M R Passos-Bueno; A H Vieira; M Vainzof; M Gill; V Gentil
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

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