The purpose of this study was to analyze the shape of the sella turcica in a group of patients with Down syndrome and compare the findings with those made earlier in human fetuses with Down syndrome. Profile radiographs from 78 patients (age 4 months to 50 3/12 years) were analyzed. A tracing was made of each sella turcica, and the shape was compared with that of a normal sella, including the normal growth pattern from childhood to adulthood. Sella turcica structure could be classified into three morphological types, defined as: type I, almost normal appearance; type II, deviations in the anterior wall; and type III, deviations in the floor of the sella turcica. Compared with previously registered prenatal structural deviations in the sella turcica, it can be concluded that the postnatal radiographic material reflects the prenatal findings, because type I, both prenatally and postnatally, is by far the most common, whereas the remaining types are uncommon, both prenatally and postnatally. The study confirms the relevance of prenatal investigations for postnatal diagnostics as previously documented in sella turcica analyses of prenatal and postnatal myelomeningocele cases.

No abstract

We studied the frequency and pattern of tooth agenesis in a Danish population with Down syndrome, trisomy 21 (46 females and 54 males). The control group consisted of a normal Danish population (2424 females and 2431 males) [Rølling, 1980: Scand J Dent Res 88:365-369; Ravn and Nielsen, 1973: Tandlaaegebladet 77:12-22]. We found that individuals with Down syndrome have an occurrence of agenesis that is some 10 times greater that in the general population with a higher frequency in males than in females. Agenesis occurred more frequently in the mandible than in the maxilla and most often on the left side. The highly significant differences were primarily found in the occurrence of agenesis of the mandibular central incisors, followed by the maxillary lateral incisors and second premolars and the mandibular second premolars. The main components in the pattern of agenesis observed in Down syndrome are supposed to be related to the peripheral nervous system and abnormal cartilagenous tissue. The present study on Down syndrome suggests that the dentition, with its many different anomalies, from agenesis to malformation, can be used as an indicator in evaluating different aspects in the patheogenetic of aneuploidy conditions.

The purpose of this dinical study was to evaluate the efFect of a 3-min daily toothbrushing with 1 % chiorhexidine gluconate toothpaste on dental plaque, gingivitis and gingival hyperplasia in 30 mentally retarded epileptic children treated with phenytoin. A double-blind cross-over technique was used. Brushing once daily for 2 months with 1% chiorhexidine gluconate toothpaste resulted in significantly lower Pi I and GI values. Gingival hyperplasia was not significantly reduced by tlie use of the chiorhexidine toothpaste.

The frequency, gender, and maxillary/mandibular occurrences of third molar agenesis have been studied in a Danish population of Down syndrome individuals (39 F and 31 M). The study was based on radiological examination and compared with 2 control groups of normal Caucasian populations. We found that the occurrence of third molar agenesis in Down syndrome individuals was around 4 times greater than in a normal population and higher than in corresponding previous studies. The agenesis occurred more often in the maxilla than in the mandible, and the frequency was not significantly higher in females than in males. The present study stresses the importance of focusing on the dental germs in the phenotypic discussion, as different genes are involved in tooth formation. The absence of teeth can contribute to an understanding of the interaction between genotype and phenotype.