Worster-Drought syndrome: poorly recognized despite severe and persistent difficulties with feeding and speech

被引:23
作者
Clark, Maria [1 ,2 ]
Harris, Rebecca [1 ]
Jolleff, Nicola [1 ]
Price, Katie [1 ]
Neville, Brian G. R. [2 ]
机构
[1] Great Ormond St Hosp Sick Children, NHS Trust, London WC1N 3JH, England
[2] UCL, Inst Child Hlth, Neurosci Unit, London WC1E 6BT, England
关键词
CEREBRAL-PALSY; CHILDREN; INVOLVEMENT;
D O I
10.1111/j.1469-8749.2009.03475.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aim Worster-Drought syndrome (WDS), or congenital suprabulbar paresis, is a permanent movement disorder of the bulbar muscles causing persistent difficulties with swallowing, feeding, speech, and saliva control owing to a non-progressive disturbance in early brain development. As such, it falls within the cerebral palsies. The aim of this study was to describe the physical and neuropsychological profiles of children with WDS. Method Forty-two children with WDS (26 males, 16 females; mean age 7y 10mo, SD 3y 1mo; range 2y 6mo to 16y 5mo) were studied prospectively using a standard protocol. Results All of the children had severe bulbar dysfunction; 36 out of 42 had feeding difficulties and 23 of 38 had unintelligible speech, which was poorly compensated for by augmentative communication. There were accompanying disturbances in cognition (mean non-verbal IQ 59), behaviour (12/40 attention-deficit-hyperactivity disorder [ADHD]), social communication (8/42 autism), and epilepsy (12/39). The severity of bulbar dysfunction and impact of additional impairments made it difficult to use formal assessments. Interpretation WDS causes severe and persistent bulbar dysfunction that is often accompanied by additional impairments, as in other cerebral palsies. Speech prognosis is particularly poor. Early diagnosis with appreciation of the underlying neurology would encourage critical evaluation of interventions and long-term planning to improve outcome.
引用
收藏
页码:27 / 32
页数:6
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