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 16 Number 1
- 발행연도
- 2020.6
- 수록면
- 27 - 34 (8page)
이용수
초록· 키워드
오류제보하기
Epidermolysis Bullosa (EB) is a rare genetic disease that causes pain and results in peeling of the skin and mucous membranes, as well as easy blistering due to minor trauma or friction. EB is classified into four types according to the layer where the tissue is desquamated and blisters form. There are three genetic disorder-type EB diseases, namely, epidermolysis bullosa simplex (EBS), junctional epidermolysis bullosa (JEB), and dystrophic epidermolysis bullosa (DEB), as well as an acquired autoimmunity disorder. DEB shows autosomal recessive or dominant inheritance, and is characterized by deformities in the skin including coalescence of the fingers, blisters, scars, abnormalities of the fingertips, and milia. In extreme cases, a narrow esophagus or airway, ankyloglossia, microglossia, or squamous cell carcinoma may be seen. Dental problems associated with EB include microstomia or ankyloglossia, caused by scarring due to repeated blistering, as well as a high risk of dental caries due to difficulty in controlling a toothbrush (in turn due to hand and finger scarring). Therefore, continuous regular examination and preventive care are important. In this case report, we describe the dental treatment applied under general anesthesia for rampant caries in a 9-year-old patient with DEB who visited Chosun University Dental Hospital.
목차
Introduction
Case Report
Discussion
Summary
References
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