지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 저널정보
- Asia Association for Disability and Oral Health International Journal of Disability and Oral Health International Journal of Disability and Oral Health Volume 17 Number 1
- 발행연도
- 2021.6
- 수록면
- 21 - 26 (6page)
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초록· 키워드
오류제보하기
Pompe disease is a rare glycogen storage disease with a lysosomal metabolism defect and autosomal recessive trait. Patient with Pompe diseases shows typical craniofacial characteristics such as facial muscle weakness and altered orofacial growth. This report presents the case of a child with the infantile-onset type of Pompe disease who receive successful orthodontic treatment with myofunctional therapy to treat malocclusion. A 10-year-old boy with Pompe disease was diagnosed as anterior crossbite with hypotonic tongue and orofacial muscle in the Department of Pediatric Dentistry, Seoul National University Dental Hospital. Orthodontic treatment using 2x4 fixed appliance followed by Frankel III appliance was done. Also, myofunctional therapy was conducted to improve the position of tongue and orofacial muscle strength. The patient was well adapted to the appliance, and the malocclusion was successfully treated without relapse. Both patient and his caregivers were very satisfied with the results.
목차
Introduction
Case report
Discussion
References
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