Literature DB >> 24592905

Craniofacial features of patients with sickle cell anemia and sickle cell trait.

Matheus Melo Pithon1, Láiza Michele Vieira Palmeira, Ana Angélica Leal Barbosa, Rafael Pereira, Ana Carolina Dias Viana de Andrade, Raildo da Silva Coqueiro.   

Abstract

OBJECTIVE: To identify the craniofacial characteristics of patients with sickle cell trait (SCT) and sickle cell anemia (SCA) and to compare these measurements with those of nonaffected subjects.
MATERIALS AND METHODS: Clinically normal patients and those with SCT and SCA were evaluated in this study. The patients were divided into three groups: normal (control), SCA, and SCT (n  =  with 15 in each group). Inclusion criteria were SCA or SCT verified by laboratory methods and no treatment with fixed orthodontics or facial orthopedics. Lateral cephalometric radiographs were carried out and were used to obtain angular and linear measurements of anatomic structures displayed. All markings and measurements were performed by a single examiner.
RESULTS: The average ANB was increased in groups with SCA (5.47 ± 2.0°) and SCT (3.80 ± 1.4°), indicating a tendency to Class II. The mean SNA angle was 83.0 ± 3.8° and 82.1±3.5° for SCA and SCT, indicating a proper positioning of the jaw from the skull base. There was an interaction between the group and sex factors for the variable SN-GoGn; measures were higher for men in the SCA group.
CONCLUSION: Patients with SCA and SCT exhibited characteristics of Class II skeletal pattern because of mandibular retrusion. Most patients showed no compensatory maxillary expansion, which was determined by the normal jaw length and absence of maxillary protrusion.

Entities:  

Keywords:  Cephalometry; Sickle cell anemia; Sickle cell trait

Mesh:

Year:  2014        PMID: 24592905      PMCID: PMC8641266          DOI: 10.2319/101513-764.1

Source DB:  PubMed          Journal:  Angle Orthod        ISSN: 0003-3219            Impact factor:   2.079


  18 in total

1.  Orthodontic treatment in a patient with sickle cell anemia.

Authors:  Matheus Melo Pithon
Journal:  Am J Orthod Dentofacial Orthop       Date:  2011-11       Impact factor: 2.650

2.  Sickle cell gnathopathy: radiologic assessment.

Authors:  D L Brown; J I Sebes
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1986-06

3.  Cephalofacial characteristics of North American Black individuals with sickle cell disease.

Authors:  L A Altemus; C W Epps
Journal:  Q Natl Dent Assoc       Date:  1974-07

4.  Oral manifestations of hemoglobinopathies. A case of homozygous hemoglobin C disease diagnosed as a result of dental radiographic changes.

Authors:  C L Halstead
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1970-11

5.  Cephalometric study of American black children with sickle-cell disease.

Authors:  H I Shnorhokian; D C Chapman; M M Nazif; T G Zullo
Journal:  ASDC J Dent Child       Date:  1984 Nov-Dec

Review 6.  Orthodontic treatment of patients with sickle-cell anemia.

Authors:  Patricia Valéria Milanezi Alves; Daniele Karina M Alves; Margareth Maria Gomes de Souza; Sandra Regina Torres
Journal:  Angle Orthod       Date:  2006-03       Impact factor: 2.079

7.  Facial features of patients with sickle cell anemia.

Authors:  Naiara Gonçalves Maia; Luís Antônio dos Santos; Ricardo D Coletta; Patrícia Helena Mendes; Paulo Rogério Bonan; Leonardo Batista Maia; Hercílio Martelli Junior
Journal:  Angle Orthod       Date:  2011-01       Impact factor: 2.079

8.  Beta-S globin haplotypes in patients with sickle cell anemia: one approach to understand the diversity in Brazil.

Authors:  Jéssika Viviani Okumura; Clarisse Lopes de Castro Lobo; Claudia Regina Bonini-Domingos
Journal:  Rev Bras Hematol Hemoter       Date:  2013

9.  Sickle cell trait: is there an increased VTE risk in pregnancy and the postpartum?

Authors:  Sofya Pintova; Hillel W Cohen; Henny H Billett
Journal:  PLoS One       Date:  2013-05-22       Impact factor: 3.240

10.  Protective effect of flavonoids against reactive oxygen species production in sickle cell anemia patients treated with hydroxyurea.

Authors:  Railson Henneberg; Michel Fleith Otuki; Aline Emmer Ferreira Furman; Priscila Hermann; Aguinaldo José do Nascimento; Maria Suely Soares Leonart
Journal:  Rev Bras Hematol Hemoter       Date:  2013
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  2 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.  Craniofacial geometric morphometrics in the identification of patients with sickle cell anemia and sickle cell trait.

Authors:  Warli de Brito Ferreira; Lorena Andrade Nunes; Matheus Melo Pithon; Lucianne Cople Maia; Cezar Augusto Casotti
Journal:  Hematol Transfus Cell Ther       Date:  2019-12-05
  2 in total

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