Plaque removal by manual and electric toothbrushing among children.

The purpose of this study was to compare the effectiveness of plaque control performed with electric and manual toothbrushes. Fifteen children with primary dentition and 14 children with mixed dentition were divided in two groups and randomly assigned to utilize a manual or an electric toothbrush. In the first session, professional plaque removal was performed, and the children spent 24 hours without brushing their teeth. In the second session, plaque was disclosed and assessed on all facial and lingual surfaces. After that, all children brushed their teeth with the predetermined toothbrush. The next procedure was the disclosure and measurement of residual plaque. After a period of 7 days, the children switched the kind of toothbrush, and the same procedures were repeated. According to the statistical analysis of the results, there were no significant differences concerning plaque removal when the toothbrushes were utilized by children with mixed dentition. On the other hand, the electric toothbrush promoted significantly greater plaque removal on the lingual surfaces of teeth from children with primary dentition.

[A case of 9p partial monosomy caused by paternal translocation. Clinical and cytogenetic aspects]. / Un caso di monosomia parziale 9p- da traslocazione paterna. Aspetti clinici e citogenetici.

The authors describe a case of partial monosomy 9p in a newborn infant, with breakpoint in the region p221, due to a father's balanced translocation with karyotype 46 XY t(9;16)(p221;q224). The phenotypical features of our patient reproduce those reported in other 35 cases described up to now in the literature: trigonocephaly, upward slanting palpebral fistures, little and horizontal mouth, disproportionally long fingers and toes. Some peculiar clinical and cytogenetical features of the case are discussed, particularly the early closure of the sternal body ossification centers (already detected during the prenatal life), the partial agenesia of the splenium corporis callosi and the partial anomalous pulmonary venous return. The Authors point out the importance of an early diagnosis, based on the awareness to the clinical abnormalities and dysmorphisms, in order to provide for an adequate and opportune genetic counseling.

Molecular cloning of a t(11;14)(q13;q32) translocation breakpoint centromeric to the BCL1-MTC.

In B-cell malignancies, the t(11;14)(q13;q32) at the 11q13 BCL1 locus is characterized by a scattering of breakpoint sites along a 100 kb genomic region, between the BCL1 major translocation cluster (MTC) and the PRAD1 (also termed cyclin D1 or CCND1) gene. Recently, the 11q13 breakpoint region was extended on both sides, centromeric to the MTC and telomeric to PRAD1. We report here the molecular cloning of a new t(11;14) breakpoint site, 20 kb centromeric to the MTC, from a patient with prolymphocytic leukemia. We subcloned a non-repetitive DNA fragment near the breakpoint and mapped this new 11q13 probe (pHO11c) relative to already identified breakpoint sites, using long- and short-range physical mapping within the BCL1 locus. Rearrangements in the BCL1 locus are associated with deregulation of the PRAD1 gene, which is often overexpressed, particularly in mantle-cell malignancies. The detectable but weak PRAD1 expression in the case we present suggests that this breakpoint centromeric to the MTC still lies inside the BCL1 locus boundaries. We think that attention should be focused on this region centromeric to the BCL1-MTC, where the investigation of previously unidentified translocations may increase understanding of the PRAD1 gene deregulation in t(11;14) associated pathologies.