76 In these disorders, anticipation has recently been shown to correlate with the expansion of trinucleotide repeat sequences

at the disease locus (Figure 1). These diseases represent a class of disorders caused by unstable DNA sequences that can change in each generation, accounting for anticipation. The discovery in rapid succession of several diseases caused by expansion of triplets raises the possibility that additional neuropsychiatrie disorders with clinical features of anticipation could be candidates.77 The common properties of Inhibitors,research,lifescience,medical these mutations are the departures from mcndclian inheritance and the highly variable phenotype with wide-ranging age at onset, which are wellknown characteristics of schizophrenia. More direct analyses of the genome have been made in order to detect large expansion of triplets in Inhibitors,research,lifescience,medical severe and early forms of schizophrenia, with conflicting and, above all, negative results.78-96 The complexity of the methods

required to detect a specific unstable mutation, and the clinical and genetic heterogeneity of schizophrenia, probably explain the presence of many negative studies and nonreplications of initially AZD9291 EGFR positive PD173955? associations. On the other hand, epidemiological evidence in favor of anticipation can be considered as very good, because it is based on many different samples Inhibitors,research,lifescience,medical and with numerous different methodological strategies. Nevertheless, the relationship between epidemiological anticipation and unstable genes remains to be proven in schizophrenia. Evidence for the anticipation effect is reinforced by the presence of a correlation for age at Inhibitors,research,lifescience,medical onset within sibships in our sample, with a younger age at onset in recent generations. If the PHC syndrome is considered as a moderate form of schizophrenia (with moderate negative features and late age at onset), then Inhibitors,research,lifescience,medical it could be associated with a low number of triplet repeats (but above the normal range). The absence of affected ascendants and the 2.4% frequency of affected descendants are in accordance with this hypothesis. Conclusion

AV-951 Clinical, epidemiological, and possibly etiopathogenic factors may thus distinguish PHC from schizophrenia. The diagnosis of PHC is mainly classified under schizophrenic disorders (paranoid type) according to DSM-IV,3 hampering the retrieval of these cases. According to DSM-IV, schizophrenia appears to be fundamentally heterogeneous and presumably consists of a group of related disorders.8 While cases of schizophrenia with onset after age 45 are mentioned, in the same way as early-onset cases, they are associated with a higher proportion of women, better occupational and marital histories, more paranoid delusions and hallucinations, and less disorganization and negative symptoms. PHC might represent a more homogeneous entity with precise clinical characteristics.