Craniofacial bone abnormalities and malocclusion in individuals with sickle cell anemia: a critical review of the literature
CPS Costa, HLCC Carvalho, EBAF Thomaz… - Revista Brasileira de …, 2012 - SciELO Brasil
This study aims to critically review the literature in respect to craniofacial bone abnormalities
and malocclusion in sickle cell anemia individuals. The Bireme and Pubmed electronic …
and malocclusion in sickle cell anemia individuals. The Bireme and Pubmed electronic …
[HTML][HTML] Enamel defects and tooth eruption disturbances in children with sickle cell anemia
CMI Lopes, MC Cavalcanti, AC ALVES E LUNA… - Brazilian oral …, 2018 - SciELO Brasil
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 …
present oral manifestations such as delayed tooth eruption and hypomineralized enamel …
Orofacial manifestations in patients with sickle cell anemia.
PHC Mendes, NG Fonseca… - Quintessence …, 2011 - search.ebscohost.com
Objective: To compare the prevalence of orofacial manifestations between patients with and
without sickle cell anemia and to investigate the distribution of such events in patients with …
without sickle cell anemia and to investigate the distribution of such events in patients with …
Craniofacial and occlusal features of children with sickle cell disease compared to normal standards: a clinical and radiographic study of 50 paediatric patients
Purpose To evaluate craniofacial and occlusal features of children with sickle cell disease
and compare them with the normal healthy children. Methods A total of 50 children …
and compare them with the normal healthy children. Methods A total of 50 children …
Saúde bucal em portadores da anemia falciforme
MJ Rodrigues, VA Menezes… - RGO. Revista Gaúcha …, 2013 - revodonto.bvsalud.org
RESUMO A anemia falciforme é a doença mais comum entre as hemoglobinopatias no
Brasil e no mundo, sendo caracterizada pela presença da hemoglobina anômala S (ou …
Brasil e no mundo, sendo caracterizada pela presença da hemoglobina anômala S (ou …
Oral health-related quality of life of children and teens with sickle cell disease
MLMF Fernandes, I Kawachi, AM Fernandes… - Revista brasileira de …, 2016 - SciELO Brasil
ABSTRACT BACKGROUND: Children with sickle cell disease may have their quality of life
affected by oral alterations. However, there is still little data on oral health-related quality of …
affected by oral alterations. However, there is still little data on oral health-related quality of …
Evaluation of the maxillomandibular positioning in subjects with sickle-cell disease through 2-and 3-dimensional cephalometric analyses: A retrospective study
HLR Dos Santos, I da Silva Barbosa, TFL de Oliveira… - Medicine, 2018 - journals.lww.com
Abstract Sickle-cell disease (SCD), which involves morphological changes to the red blood
cells, is the most common hemoglobinopathy worldwide. This conformational change in …
cells, is the most common hemoglobinopathy worldwide. This conformational change in …
Manifestações bucais em pacientes portadores de anemia: estudo clínico e radiográfico
WP Jacomacci, CH Gibim, TT Higa… - Revista da Faculdade …, 2014 - seer.upf.br
Manifestações bucais da anemia estão entre os diversos sinais e sintomas associados à
doença, tornando a participação do cirurgião dentista de fundamental importância no …
doença, tornando a participação do cirurgião dentista de fundamental importância no …
Health-related quality of life in children and adolescents with sickle cell disease
GAR Veras, CMI Lopes, ACA e Luna… - Research, Society and …, 2020 - rsdjournal.org
To assess the health-related quality of life of children and adolescents with sickle cell
disease (SCD). This is a cross-sectional study carried out with 97 male and female patients …
disease (SCD). This is a cross-sectional study carried out with 97 male and female patients …
Oral changes in patients with sickle cell anemia of dentistry interest
MGP da Silva, CA Leite… - Journal of …, 2018 - … .pgsskroton.com.br
Sickle cell anemia is determined by the presence of S hemoglobin in homozygous,
autosomal recessive and characterized by the presence of red cells with abnormal shape …
autosomal recessive and characterized by the presence of red cells with abnormal shape …