| Literature DB >> 20554999 |
Leopoldo Silva de Moraes1, André Salim Khayat, Patrícia Danielle Lima de Lima, Eleonidas Moura Lima, Giovanny Rebouças Pinto, Mariana Ferreira Leal, Marília de Arruda Cardoso Smith, Rommel Rodríguez Burbano.
Abstract
The identification of cytogenetic abnormalities in schizophrenic patients may provide clues to the genes involved in this disease. For this reason, a chromosomal analysis of samples from 62 schizophrenics and 70 controls was performed with trypsin-Giemsa banding and fluorescence in situ hybridization of the X chromosome. A clonal pericentric inversion on chromosome 9 was detected in one male patient, and we also discovered mosaicism associated with X chromosome aneuploidy in female patients, primarily detected in schizophrenic and normal female controls over 40 years old. When compared with age-matched female controls, the frequency of X chromosome loss was not significantly different between schizophrenics and controls, except for the 40- to 49-year-old age group. Our findings suggest that the X chromosome loss seen in schizophrenic patients is inherent to the normal cellular aging process. However, our data also suggest that X chromosome gain may be correlated with schizophrenia in this Brazilian population.Entities:
Mesh:
Year: 2010 PMID: 20554999
Source DB: PubMed Journal: In Vivo ISSN: 0258-851X Impact factor: 2.155