Literature DB >> 15997262

Occlusal features of sickle cell anaemia patients in Lagos, Nigeria.

O O daCosta1, M O Kehinde, M O Ibidapo.   

Abstract

One hundred and four sickle cell anaemia patients aged 10-45 years and attending the out patients' clinic of the Lagos University Teaching Hospital as part of a routine check-up were seen. They were in a steady state of health. By means of a structured questionnaire the Biodata of each consecutive eligible patient was obtained and physical examination was carried out. Oral examination was done with emphasis on occlusal variables including Angle's Classification of occlusion, overjet, overbite, tooth: bone ratio, lip competence and skeletal pattern. Results showed that the majority of the patients 92 (88.5%) seen presented with Angle's Class 1 malocclusion. Increased overjet was observed in 50 (48.2%) of the sample population while an overbite depth of 2 was most frequently seen in these patients. Spacing in the anterior segment of the upper and lower arches was a fairly common occurrence, occurring in 51 (49.0%) and 39 (30.8%) of the patients seen respectively. Normal dental base relationship (Skeletal 1) was observed in 72 (69.2%) while lip incompetence was seen in 41 (39.4%) of the patients examined. Occlusal anomalies vary from mild to severe and may be attributable to hyperplastic maxillary bone and the resultant skeletal discrepancy.

Entities:  

Mesh:

Year:  2005        PMID: 15997262

Source DB:  PubMed          Journal:  Niger Postgrad Med J


  5 in total

1.  Malocclusion and Craniofacial Characteristics in Saudi Adolescents with Sickle Cell Disease.

Authors:  Ahmed Basyouni; Naif Nasser Almasoud; Khalifa Sulaiman Al-Khalifa; Badr Abdulrahman Al-Jandan; Osama Abdulsalam Al Sulaiman; Muhammad Ashraf Nazir
Journal:  Saudi J Med Med Sci       Date:  2018-08-14

2.  Malocclusion and treatment need in children and adolescents with sickle cell disease.

Authors:  Ana Cláudia Alves e Luna; Fabiana Godoy; Valdenice Aparecida de Menezes
Journal:  Angle Orthod       Date:  2013-11-25       Impact factor: 2.079

3.  Craniofacial bone abnormalities and malocclusion in individuals with sickle cell anemia: a critical review of the literature.

Authors:  Cyrene Piazera Silva Costa; Halinna Larissa Cruz Correia de Carvalho; Erika Bárbara Abreu Fonseca Thomaz; Soraia de Fátima Carvalho Sousa
Journal:  Rev Bras Hematol Hemoter       Date:  2012

4.  Oral health-related quality of life of children and teens with sickle cell disease.

Authors:  Maria Luiza da Matta Felisberto Fernandes; Ichiro Kawachi; Alexandre Moreira Fernandes; Patrícia Corrêa-Faria; Saul Martins Paiva; Isabela Almeida Pordeus
Journal:  Rev Bras Hematol Hemoter       Date:  2016-02-13

5.  Comment on: "Oral health-related quality of life in children and teens with sickle cell disease".

Authors:  Maria Elvira Pizzigatti Correa
Journal:  Rev Bras Hematol Hemoter       Date:  2016-03-19
  5 in total

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