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Congenital aglossia with situs inversus totalis - A case report
Citations
SCOPUS
12초록
Hypoglossia or aglossia is an uncommon anomaly, either of which may occur as an isolated finding or in association with other deformations, especially limb anomalies. Their genetic background is uncertain, and drug induced teratogen has not been clearly identified. We experienced a case of congenital aglossia with situs inversus in a female infant aged twelve days. Her initial complaints at admission were feeding difficulty and weight loss. In a review of literature, the association with situs inversus is very rare and only three cases have been reported until now.
키워드
Congenital aglossia; Situs inversus; article; case report; congenital malformation; electrocardiography; female; genetics; human; multiple malformation syndrome; newborn; prenatal development; situs inversus; tongue; Abnormalities, Multiple; Electrocardiography; Female; Humans; Infant, Newborn; Situs Inversus; Tongue
- 제목
- Congenital aglossia with situs inversus totalis - A case report
- 저자
- Jang G.-Y.; Lee K.-C.; Choung J.-T.; Son C.-S.; Tockgo Y.-C.
- 발행일
- 1997
- 유형
- Article
- 권
- 12
- 호
- 1
- 페이지
- 55 ~ 57
- 언어
- ENG
- 출판사
- Korean Academy of Medical Science
- 발행국가
- 대한민국
- 분량
- 3 페이지
- ISSN
- E 1598-6357
P 1011-8934