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ファイル
言語
英語
著者
田草 雄一
斎藤 恭子
瀬島 斉
木村 正彦
岸 和子
秦 利之
宮崎 康二
森竹 浩三
山口 清次
内容記述(抄録等)
We described a case of Dandy-Walker syndrome, that was detected in utero and was evaluated and monitored postnatally. The prenatal examination by echography and MRI revealed a large posterior fossa cyst with splaying of the cerebellar hemispheres. The male infant was born at 40 weeks of gestation, weighing 3430g with no special problems. Although the infant presented transient tachypnea immediately after birth, he has had no neurological symptoms. Echography, computed tomography (CT) and magnetic resonance imaging (MRI) performed after birth revealed an enlargement of the fourth ventricle but not of the lateral ventricles, and dysgenesis of the cerebellar vermis. Circumference of the head was normal and no extracranial anomalies except for the left simian crease were noted. Chromosomal analysis showed normal male pattern, 46,XY. He has been carefully followed up with no neurosurgical treatment. He has showed normal growth and development, and no hydrocephalus, as of 3 months of his age.
主題
Dendy-Walker malformation
the value of prenatal diagnosis
prenatal echography
postnatel evaluation
掲載誌名
Shimane journal of medical science
16
1
開始ページ
5
終了ページ
7
ISSN
03865959
ISSN(Online)
24332410
発行日
1998-06-01
NCID
AA00841586
出版者別表記
Shimane Medical University
資料タイプ
紀要論文
ファイル形式
PDF
著者版/出版社版
出版社版
部局
医学部
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