The bitewing radiographs of 1,731 English and Danish schoolchildren aged 13--15 years were examined to assess the prevalence of chronic periodontitis. Only one child (0.06%) was found to be affected in comparison with the high prevalence of 51.5% reported by Hull et al. (1975). Minute qualitative changes in the radiographic appearance of the alveolar crest, or changes in the visual representation of the width of the periodontal ligament space are not reliable or valid criteria for assessing chronic periodontitis. Horizontal bone loss observed on radiographs, which can be accurately measured using the cemento-enamel junction as a reference point, is a useful diagnostic criterion for the measurement of chronic periodontitis.
A total of 1036 Indian children were examined to determine the mean ages of eruption for the first permanent molars, and the permanent central and lateral incisors. The youngest observed age for the eruption of any permanent tooth was 5.00 years for girls and 4.94 for boys. Mandibular teeth erupted earlier than maxillary teeth and teeth in females erupted between 1 and 6 months earlier than in males. Comparison of the results of the present study to one in South African black children showed that Indian children's teeth erupt some 3.5-7 months later than those of black children, a difference that was statistically significant.
Acrocephalopolysyndactyly Type II (Carpenter Syndrome) is determined by autosomal recessive inheritance. Only some 40 cases have been described. Variable clinical signs have been described including prolonged retention of primary teeth and hypodontia. This paper describes the oral and dental findings in a family containing two affected brothers. The family pedigree is informative, as the mother has had children by three partners. The two affected individuals are full brothers. The first affected brother has delayed dental development, severe hypodontia and small tooth crown size. Mesio-distal and bucco-lingual dimensions were measured on the study models and compared with population data. The younger brother also has delayed dental development but only mild hypodontia. Their half sister has severe hypodontia but no signs of Carpenter Syndrome. This family study demonstrates two affected individuals with typical clinical features and a pedigree compatible with autosomal recessive inheritance. Small tooth crown size has been shown by standardized measurement and evidence advanced that hypodontia is not part of the syndrome but a coincidental finding which segregates independently. We have also shown that the marked delay in emergence of teeth is associated more with problems of tooth eruption, possibly related to the bony abnormalities, than to a generalized delay in dental development.
The aim of the study was to determine the prevalence of iron-deficiency anaemia in children less than 6 years of age who attended for outpatient general anaesthesia for dental extractions. Pre-or pen-operative capillary blood samples were taken from 109 children (70 white Caucasian and 39 ethnic-minority children). The haemoglobin concentration (Hb), mean cell volume (MCV) and red cell porphyrin (RCP) value were determined for each subject. 19% of the children were found to be anaemic (Hb < 1 1 g/dl) and there was no statistically significant difference for mean Hb or prevalence of anaemia between white Caucasian and ethnic-minority children. A significantly greater proportion of the ethnic-minority children were iron deficient, as indicated by low MCV and high RCP. There were no statistically significant differences between anaemic and non-anaemic subjects with regard to sex or social class, but a significantly greater mean number of extractions were performed in the anaemic children.
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