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Clinical analysis of West syndrome associated with phenylketonuria.

机译:西方综合症与苯丙酮尿症相关的临床分析。

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OBJECTIVE: To explore the incidence and clinical characteristics of West syndrome associated with phenylketonuria (WS-PKU) and significance of early combination therapy of low phenylalanine (PHE) diet and anticonvulsants (antiepileptic drugs, AEDs) in WS-PKU. SUBJECTS AND METHODS: Sixty-two WS-PKU patients (41 boys and 21 girls) out of 503 PKU patients were enrolled in the study. Age at PKU diagnosis varied from 4 months to 7 years old. Serum PHE levels were 20-38.5mg/dl. In the majority of cases, infantile spasms (IS) became manifest first preceding the PKU diagnosis, except eight cases in which spasms appeared after starting the diet therapy. All patients were subjected to mental and electroencephalographic (EEG) examination. Brain myelination was evaluated by using brain magnetic resonance imaging (MRI) with Staudt's standard. RESULTS: WS-PKU patients accounted for 12.3% of PKU patients. No patients who were given low PHE diet before age 3 months suffered from WS, whereas 17 out of 156 patients who started the diet between age 4 and 12 months developed WS later (10.9%), and similarly, 45 out of 283 patients who started the diet after 12 months of age developed WS later (15.9%). Moderate and severe mental retardation were noted in 58.8% of patients who received the diet before age 1 and in 84.4% of those after age 1 (P<0.05). EEG displayed hypsarrhythmia and diffuse background abnormality. MRI scans showed delayed myelination mainly in the cerebral lobes and corpus callosum and abnormal high T(2)-signal intensity (100%) in the periventricular region around anterior and posterior horns of both lateral ventricles. With the start of diet, spasms began to decrease its frequency, but relapsed frequently (78%) when no AEDs were given. Seizure relapse was significantly lower when valproic acid or nitrazepam were given concomitantly with the diet (18.2%). CONCLUSIONS: IS often occurred as the initial clinical sign of PKU. Early diagnosis of PKU and early therapy with low PHE diet seem to be highly effective in preventing WS.
机译:目的:探讨与苯丙酮尿症(WS-PKU)有关的西方综合症的发生率和临床特征,以及低苯丙氨酸(PHE)饮食和抗惊厥药(抗癫痫药,AEDs)在WS-PKU中早期联合治疗的意义。研究对象和方法:研究纳入了503名PKU患者中的62名WS-PKU患者(41名男孩和21名女孩)。北大诊断的年龄从4个月到7岁不等。血清PHE水平为20-38.5mg / dl。在大多数情况下,婴儿痉挛症(IS)在PKU诊断之前首先表现出来,除了8例开始饮食治疗后出现痉挛。所有患者均接受了脑电图和脑电图检查。通过使用符合Staudt标准的脑磁共振成像(MRI)评估大脑的髓鞘形成。结果:WS-PKU患者占PKU患者的12.3%。在3个月之前没有接受过低PHE饮食的患者中没有WS,而156例在4到12个月之间开始饮食的患者中有17例后来出现了WS(10.9%),同样,在283例开始中的患者中有45 12个月大后的饮食后来发展为WS(15.9%)。在1岁之前接受饮食的患者中有58.8%的人患有中度和重度智力低下,在1岁以后接受饮食的患者中有84.4%(P <0.05)。脑电图显示心律失常和弥漫性背景异常。 MRI扫描显示,髓鞘形成延迟主要发生在脑叶和call体,两个侧脑室前后角周围的脑室周围区域异常高的T(2)信号强度(100%)。随着饮食的开始,痉挛开始减少其频率,但是当没有给予AED时,痉挛经常复发(78%)。饮食中同时服用丙戊酸或硝西epa时,癫痫发作的复发率显着降低(18.2%)。结论:IS常作为PKU的初始临床体征出现。 PKU的早期诊断和低PHE饮食的早期治疗似乎对预防WS非常有效。

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