Marfan syndrome (MFS) is a type of connective tissue disorder caused by a mutation of the fibrillin gene and increased TGF-β in tissues. This disorder leads to connective tissue fragility, with such clinical manifestations as slender fingers, long limbs, abnormal cardiac valves, and aortic aneurysm development. We present here a case of Class II maxillary protrusion in a 13-year-old male with MFS. The patient underwent orthodontic treatment, including extractions of the upper and lower bicuspids. The treatment achieved a good Class I occlusion with normal overjet and overbite. On the other hand, we found extraordinary craniofacial skeleton development during the post-adolescent period and untreatable marginal gingivitis despite complete plaque control, which might be resulted from connective tissue fragility.
CITATION STYLE
Kawakami, M., Shimomura, T., & Kirita, T. (2019). Orthodontic management of patient with marfan syndrome - case report and review of the literature. International Journal of Dentistry and Oral Science, 6(2), 676–680. https://doi.org/10.19070/2377-8075-19000133
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