Robinow 증후군 환아의 전신마취를 이용한 치료증례보고
Treatment of the child with robinow syndrome under general anesthesia: A case report
김경석, 김신근,
소속 상세정보
김경석 ( ) - 경북대학교 의과대학 내과학교실
김신근 ( ) - 경희대학교
KMID : 0358919960230030601
Abstract
Robinow syndrome or fetal face syndrome is a rare inherited disorder characterized by short stature, mesomelic brachymelia, hypoplastic genitalia, and a typical facial appearence("fetal face") with fromtal bossing, hypertelorism, ear
abnormalities,
a
short upturned nose, long piltrum, micrognathia, and macrocephaly.
Intraoral features have included quite a few dental cavities, crowding, hypoplastic uvula, cleft lip or/and cleft palate, gingival hyperplasia, alveolar hyperplasia, enamel hypoplasia, delayed eruption, and congenital missing of the permanent
teeth.
We report on a 10 years old girl with Robinow syndrome. The patient had most of the typical anomalies of the syndrome and negative family history but, in addition, had mental retardation, hearing loss, and serous otitis media. Intraoral findings
included dental cavities, crowding, hypoplastic uvula, repaired cleft palate, and mouth breathing.
Dental treatment and V-tube insertion(by dept. of ENT) were performed under general anesthesia.
In all cases of Robinow syndrome, thorough evaluation and united treatments with medical specialists should be performed.
키워드
원문 및 링크아웃 정보
등재저널 정보