Literature DB >> 9784831

Chromosome fragile sites in mentally retarded males: increased incidence with seizures and diphenylhydantoin therapy.

K B Hodges1, R S Larson, M G Butler.   

Abstract

Chromosome fragile site or lesion data were examined in 154 institutionalized mentally retarded males with or without seizures or treated with anti-seizure medication. Blood lymphocytes were cultured using three different cell culture conditions and the incidence of specific chromosome fragile sites (10q25, 16q22, and 12q23) or lesions determined. Increased fragile sites were seen in mentally retarded males with seizures compared to those without seizures in cells grown in folate-deplete Medium 199. Those with seizures and treated with diphenylhydantoin had a higher incidence of induced fragile sites (p < 0.001) relative to similar patients treated with anti-seizure medication other than diphenylhydantoin. These results suggest that a cohort of patients with mental retardation and seizures are more likely to have induced cytogenetic changes when treated with diphenylhydantoin than mentally retarded individuals without seizures.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9784831      PMCID: PMC5292046     

Source DB:  PubMed          Journal:  Ann Clin Lab Sci        ISSN: 0091-7370            Impact factor:   1.256


  17 in total

1.  No significant relationship between age and frequency of chromosome lesions in mentally retarded individuals with or without the fragile X syndrome.

Authors:  M G Butler
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

2.  A guide to fragile sites on human chromosomes.

Authors:  F Hecht; K H Ramesh; D H Lockwood
Journal:  Cancer Genet Cytogenet       Date:  1990-01

3.  Chromosome fragility and psychopathology in obligate female carriers of the fragile X chromosome.

Authors:  L S Freund; A L Reiss; R Hagerman; S Vinogradov
Journal:  Arch Gen Psychiatry       Date:  1992-01

4.  Cytogenetic studies of males with schizophrenia. Screening for the fragile X chromosome and other chromosomal abnormalities.

Authors:  L E DeLisi; A L Reiss; B J White; E S Gershon
Journal:  Schizophr Res       Date:  1988 Jul-Aug       Impact factor: 4.939

5.  Cytogenetic studies in children on long-term anticonvulsant therapy.

Authors:  S Kitsiou-Tzeli; A Galla-Voumvouraki; A Tsezou; E Kavazarakis; A Skardoutsou; P Koukoutsakis; C Sinamniotis
Journal:  Acta Paediatr       Date:  1994-06       Impact factor: 2.299

Review 6.  Sister chromatid exchange (SCE) and structural chromosome aberration in mutagenicity testing.

Authors:  E Gebhart
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Chromosome lesions which could be interpreted as "fragile sites" on the distal end of Xq.

Authors:  M G Butler; G A Allen; J L Haynes; S J Clark
Journal:  Am J Med Genet       Date:  1990-10

8.  Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome.

Authors:  M G Butler; B B Jenkins
Journal:  Am J Med Genet       Date:  1989-04

9.  Is Rett syndrome a chromosome breakage syndrome?

Authors:  L Telvi; M Leboyer; C Chiron; J Feingold; G Ponsot
Journal:  Am J Med Genet       Date:  1994-07-15

10.  Chromosomal investigations in epileptic children during long-term therapy with phenytoin or primidone.

Authors:  K J Esser; F Kotlarek; M Habedank; U Mühler; E Mühler
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.