Literature DB >> 26529839

Oral health and oromotor function in rare diseases--a database study.

Lotta Sjögreen, Jan Andersson-Norinder, John Bratel.   

Abstract

The aim was to study oral health and oromotor function in individuals with rare diseases. A disease is defined as rare when it affects no more than 100 individuals per million population and leads to a marked degree of disability. An affected nervous or musculoskeletal system, cognitive impairment, neuropsychiatric disorders and craniofacial malformations are common in rare diseases and may all be risk factors for oral health and oromotor function. In 1996-2008, 1,703 individuals with 169 rare diseases, aged 3-67 years, answered a questionnaire about general health, oral health and orofacial function and 1,614 participated in a clinical examination. A control group of 135 healthy children, aged 3-14 years, was also included in the study. Oral health was examined by a dentist and oromotor function by a speech-language pathologist. The participants with rare diseases were recruited via family programmes, referrals to the clinic and research projects, while the controls were randomly selected from a Swedish municipality. In the diagnosis group, 40% had moderate or severe problems coping with dental treatment, 43% were receiving specialised dental care. Difficulties related to tooth brushing were common compared with the controls. Approximately two thirds of the study group and the control group were caries free. Frontal open bite, long face and high palate were common in individuals with rare diseases compared with controls. Oromotor impairment was a frequent finding (43%) and was absent among the controls. There was a significant correlation between oromotor impairment and certain structural deviations and oral-health issues. Compared with healthy controls, individuals with rare diseases often have difficulty coping with dental treatment and managing tooth brushing. Dysmorphology and oromotor dysfunction are frequent findings in this population and they often require extra prophylactic dental care and access to specialised dental care in order to prevent oral disease.

Entities:  

Mesh:

Year:  2015        PMID: 26529839

Source DB:  PubMed          Journal:  Swed Dent J        ISSN: 0347-9994


  7 in total

1.  Rare genetic diseases affecting skeletal development and oral health disparities among children and adolescents: a pathway analysis.

Authors:  Mario Vianna Vettore; Ana Cristina Borges-Oliveira; Heloisa Vieira Prado; Gabriela de Almeida Lamarca; Janine Owens
Journal:  Int Dent J       Date:  2020-07-17       Impact factor: 2.607

2.  Assessing a possible vulnerability to dental caries in individuals with rare genetic diseases that affect the skeletal development.

Authors:  Heloisa Vieira Prado; Natália Cristina Ruy Carneiro; Matheus França Perazzo; Mauro Henrique Nogueira Guimarães de Abreu; Carolina de Castro Martins; Ana Cristina Borges-Oliveira
Journal:  Orphanet J Rare Dis       Date:  2019-06-18       Impact factor: 4.123

3.  Malocclusion in children with speech sound disorders and motor speech involvement: a cross-sectional clinical study in Swedish children.

Authors:  Å Mogren; C Havner; A Westerlund; L Sjögreen; M Barr Agholme; A Mcallister
Journal:  Eur Arch Paediatr Dent       Date:  2022-07-01

4.  Children and adolescents with speech sound disorders are more likely to have orofacial dysfunction and malocclusion.

Authors:  Åsa Mogren; Anders Sand; Christina Havner; Lotta Sjögreen; Anna Westerlund; Monica Barr Agholme; Anita Mcallister
Journal:  Clin Exp Dent Res       Date:  2022-06-20

5.  Knowledge and Associated Factors about Rare Diseases among Dentists in Israel: A Cross Sectional Survey.

Authors:  Eitan Mijiritsky; Michal Dekel-Steinkeller; Oren Peleg; Shlomi Kleinman; Clariel Ianculovici; Amir Shuster; Shimrit Arbel; Menachem Ben-Ezra; Maayan Shacham
Journal:  Int J Environ Res Public Health       Date:  2021-06-25       Impact factor: 3.390

6.  Oral hygiene aspects in a study of children and young adults with the congenital and childhood forms of myotonic dystrophy type 1.

Authors:  Åsa Mårtensson; Anne-Berit Ekström; Monica Engvall; Lotta Sjögreen
Journal:  Clin Exp Dent Res       Date:  2016-08-04

7.  Rare Disorders: Diagnosis and Therapeutic Planning for Patients Seeking Orthodontic Treatment.

Authors:  Carolina Arriagada-Vargas; María Teresa Abeleira-Pazos; Mercedes Outumuro-Rial; Eliane García-Mato; Iván Varela-Aneiros; Jacobo Limeres-Posse; Pedro Diz-Dios; Márcio Diniz-Freitas
Journal:  J Clin Med       Date:  2022-03-10       Impact factor: 4.241

  7 in total

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