CNS malformation in a child with Kabuki (Niikawa-Kuroki) syndrome: Report and review

Da Chang Chu, Sara C. Finley, Daniel W. Young, Virginia K. Proud*

*此作品的通信作者

研究成果: 期刊稿件文章同行評審

37 引文 斯高帕斯(Scopus)

摘要

Kabuki (Niikawa-Kuroki) syndrome (KS) comprises characteristic facial changes, developmental delay, skeletal anomalies, mental retardation, and abnormal dermatoglyphics. We report on a 5-year-old Caucasian boy with KS who required surgery for a giant left temporoparietal subarachnoid cyst at age 5 1/4 years. Review of the 143 published cases shows that while malformations may be found in the endocrine, cardiac, genitourinary and skeletal systems, this is the first case of Kabuki syndrome with a major central nervous system malformation.

原文英語
頁(從 - 到)205-209
頁數5
期刊American Journal of Medical Genetics
72
發行號2
DOIs
出版狀態已出版 - 17 10 1997
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