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1.
Braz Oral Res ; 32: e87, 2018 Aug 13.
Article in English | MEDLINE | ID: mdl-30110085

ABSTRACT

Sickle cell anemia, a genetic disease caused by a mutation in the beta-globin gene, can present oral manifestations such as delayed tooth eruption and hypomineralized enamel and dentin. The aim of the present study was to evaluate the prevalence and severity of developmental defects of enamel (DDE) and delayed tooth eruption in children with sickle cell anemia. The sample comprised 56 male and female children with sickle cell anemia aged 6 to 12 years and treated at the Hematology and Hemotherapy Center of Pernambuco, Brazil. The data were collected according to the WHO criteria for DDE and tooth eruption. The prevalence of DDE was 58.2% and increased with age, affecting 43.8% of children aged 6 to 8 years and 66.7% of those aged 10 to 12 years (p>0.05; Pearson's chi-square test). There was no significant association between DDE and sex; the most prevalent type of DDE was diffuse opacity (6.2%). Tooth eruption was delayed in 18 children (32.1%). The delay increased with age and was detected in 11.8% of children aged 6 to 8 years, in 20.0% of those aged 8 to 10 years and in 54.2% of those aged 10 to 12 years (p<0.05; Pearson's chi-square test). Delayed tooth eruption was higher in males (36.7%, p>0.05). The prevalence of DDE was high, increased with age and was similar between sexes, while delayed eruption was higher in males and showed a significant association with age.


Subject(s)
Anemia, Sickle Cell/epidemiology , Dental Enamel/abnormalities , Tooth Diseases/epidemiology , Tooth Eruption , Age Distribution , Age Factors , Anemia, Sickle Cell/complications , Brazil/epidemiology , Child , Cross-Sectional Studies , Dental Enamel Hypoplasia/epidemiology , Dental Enamel Hypoplasia/etiology , Female , Humans , Male , Prevalence , Severity of Illness Index , Sex Distribution , Sex Factors , Tooth Diseases/etiology
2.
Braz. oral res. (Online) ; 32: e87, 2018. tab
Article in English | LILACS | ID: biblio-952168

ABSTRACT

Abstract Sickle cell anemia, a genetic disease caused by a mutation in the beta-globin gene, can present oral manifestations such as delayed tooth eruption and hypomineralized enamel and dentin. The aim of the present study was to evaluate the prevalence and severity of developmental defects of enamel (DDE) and delayed tooth eruption in children with sickle cell anemia. The sample comprised 56 male and female children with sickle cell anemia aged 6 to 12 years and treated at the Hematology and Hemotherapy Center of Pernambuco, Brazil. The data were collected according to the WHO criteria for DDE and tooth eruption. The prevalence of DDE was 58.2% and increased with age, affecting 43.8% of children aged 6 to 8 years and 66.7% of those aged 10 to 12 years (p>0.05; Pearson's chi-square test). There was no significant association between DDE and sex; the most prevalent type of DDE was diffuse opacity (6.2%). Tooth eruption was delayed in 18 children (32.1%). The delay increased with age and was detected in 11.8% of children aged 6 to 8 years, in 20.0% of those aged 8 to 10 years and in 54.2% of those aged 10 to 12 years (p<0.05; Pearson's chi-square test). Delayed tooth eruption was higher in males (36.7%, p>0.05). The prevalence of DDE was high, increased with age and was similar between sexes, while delayed eruption was higher in males and showed a significant association with age.


Subject(s)
Humans , Male , Female , Child , Tooth Diseases/epidemiology , Tooth Eruption , Dental Enamel/abnormalities , Anemia, Sickle Cell/epidemiology , Tooth Diseases/etiology , Severity of Illness Index , Brazil/epidemiology , Sex Factors , Prevalence , Cross-Sectional Studies , Age Factors , Sex Distribution , Age Distribution , Dental Enamel Hypoplasia/etiology , Dental Enamel Hypoplasia/epidemiology , Anemia, Sickle Cell/complications
3.
Angle Orthod ; 84(3): 467-72, 2014 May.
Article in English | MEDLINE | ID: mdl-24274957

ABSTRACT

OBJECTIVE: To assess the prevalence of malocclusion and treatment need in children and adolescents with sickle cell disease (SCD). MATERIALS AND METHODS: In this cross-sectional study, the sample size comprised 35 five-year-old children and 36 adolescents of both sexes, aged between 12 to 18 years, with SCD. Dental occlusion was assessed using two indexes: the Malocclusion Index (World Health Organization) and the Dental Aesthetic Index (DAI). RESULTS: The prevalence of malocclusion in the preschool children was 62.9%. The main malocclusions observed in this age group were Class II (37.1%), increased overjet (28.6%), reduced overbite (28.6%), and open bite (17.1%). In the 12- to 18-year-old subjects, the prevalence of malocclusion was 100%, and the most prevalent types of malocclusion were maxillary overjet (63.9%) and maxillary misalignment (58.3%). It is noteworthy that the majority of adolescents (80.6%) had very severe or disabling malocclusions. CONCLUSION: The results revealed a high prevalence of malocclusion in children and adolescents with SCD. According to DAI score, the majority of the sample presented with very severe malocclusion and a compulsory treatment need.


Subject(s)
Anemia, Sickle Cell/epidemiology , Malocclusion/epidemiology , Needs Assessment/statistics & numerical data , Adolescent , Age Factors , Brazil/epidemiology , Child , Child, Preschool , Cross-Sectional Studies , Educational Status , Epidemiologic Studies , Esthetics, Dental , Female , Humans , Income/statistics & numerical data , Male , Malocclusion, Angle Class I/epidemiology , Malocclusion, Angle Class II/epidemiology , Open Bite/epidemiology , Overbite/epidemiology , Parents/education , Prevalence , Residence Characteristics/statistics & numerical data , Tooth Loss/epidemiology
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