- 영문명
- Clinical Features of Partial Agenesis of Corpus Callosum
- 발행기관
- 대한소아신경학회
- 저자명
- 김순남(Soon Nam Kim) 차병호(Byung Ho Cha) 이준수(Joon Soo Lee) 고창준(Chang Jun Coe)
- 간행물 정보
- 『Annals of Child Neurology(구 대한소아신경학회지)』대한소아신경학회지 제2권 제2호, 18~25쪽, 전체 8쪽
- 주제분류
- 의약학 > 의학일반
- 파일형태
- 발행일자
- 1995.05.20

국문 초록
영문 초록
59 cases with partial agenesis of corpus callosum visited to Department of pediatrics. College of medicine, Yonsei university, from Jan.1980 to Dec.1993, were reviewed on the basis of clinical characteristics.
The results were summarized as follows: the age distribution were 31 cases(52.5%) under 1year, 20 cases(33.8%) from 1 to 5 years, 8 cases(13.7%) from 6 to 15 years. Sex distribution revealed males to females to be 1:1.2. All cases shewed mental retardation, 30 cases(50.8%) with seizure, 8 cases(13.6%) with cerebral palsy, and the most common type of seizure was generalized tonic clonic seizure. 24 of 56 patients had abnormal perinatal history: 22% of them had perinatal asphyxia, 10%. low birth weight, 6.7%. prematurity. 48 patients had associated anomalies. among which craniofacial anomaly was the most common and 8 patients had cardiovascular. 8 patients, skeletal anomalies. We used Griffith developmental scale to assess the developmental status in 31 cases. None of the cases achieved the score above 85 for general intelligence quotient and 24 cases were below 55. EEG revealed most commonly asymmetricity between two hemispheres. some of them showed spikes and slow waves.
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