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

作者信息

Chu D C, Finley S C, Young D W, Proud V K

机构信息

Laboratory of Medical Genetics, University of Alabama at Birmingham, USA.

出版信息

Am J Med Genet. 1997 Oct 17;72(2):205-9.

PMID:9382144
Abstract

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 1/2 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.

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