Title |
Marfan syndrome: a review of the literature and case report
|
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Published in |
Special Care in Dentistry, February 2013
|
DOI | 10.1111/scd.12018 |
Pubmed ID | |
Authors |
Annetta K. L. Tsang, Aart Taverne, Trevor Holcombe |
Abstract |
Marfan syndrome (MFS) is a connective tissue disorder of variable inheritance that affects multiple organ systems. Cardiovascular, ocular, and skeletal abnormalities are cardinal features of the syndrome. Orofacially, MFS patients typically exhibit skeletal class II malocclusion, dolichofacial growth pattern, mandibular retrognathia, malar hypoplasia, high arched palate, dental crowding, and root anomalies. The purpose of this paper is to provide a review of the literature, as well as describe an 11-year-old female with MFS diagnosed at the age of 10.5 years. This report emphasizes the orofacial findings in MFS and highlights particularities of dental treatment when social deficits and intellectual disabilities are also implicated. |
X Demographics
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 1 | 2% |
Unknown | 45 | 98% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 10 | 22% |
Student > Master | 9 | 20% |
Student > Doctoral Student | 4 | 9% |
Researcher | 4 | 9% |
Student > Bachelor | 4 | 9% |
Other | 5 | 11% |
Unknown | 10 | 22% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 24 | 52% |
Agricultural and Biological Sciences | 7 | 15% |
Nursing and Health Professions | 3 | 7% |
Psychology | 1 | 2% |
Unknown | 11 | 24% |