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 |
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頁(從 - 到) | 205-209 |
頁數 | 5 |
期刊 | American Journal of Medical Genetics |
卷 | 72 |
發行號 | 2 |
DOIs | |
出版狀態 | 已出版 - 17 10 1997 |
對外發佈 | 是 |