Juvenile neuronal ceroid lipofuscinosis (Batten disease): current insights.

Degenerative Neurological and Neuromuscular Disease Pub Date : 2016-08-01 eCollection Date: 2016-01-01 DOI:10.2147/DNND.S111967
John R Ostergaard
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引用次数: 40

Abstract

The present review is focused on juvenile neuronal ceroid lipofuscinosis (JNCL; Batten disease) due to a mutation in CLN3. Functional vision impairment occurring around 5-6 years of age is the first symptom in more than 80% of patients. Approximately 2 years later (though sometimes simultaneously), obvious signs of cognitive impairment appear. Behavior problems can occur in advance, especially in boys. These include anxious and depressed mood, aggressive behavior, and hallucinations, and even psychotic symptoms. Following the teens, severe dementia is present, including loss of memory, attention, and general reasoning abilities, as well as loss of independent adaptive skills such as mobility, feeding, and communicating. Sleep abnormalities, such as settling problems, nocturnal awakenings, and nightmares, are reported in more than half of patients. The vast majority, if not all, patients develop seizures, starting at approximately 10 years of age. Generalized tonic-clonic seizure occurs as the only type of seizure in approximately half of patients, and in combination with partial seizures in a third of patients. There seems to be no difference in seizure severity according to sex or genotype, and there is great variation in seizure activity among patients. Soon after diagnosis, patients begin to have slight ataxic symptoms, and at adolescence extrapyramidal symptoms (rigidity, bradykinesia, slow steps with flexion in hips and knees) occur with increasing frequency. Chewing and swallowing difficulties emerge as well, and food intake is hampered in the late teens. Disabling periodically involuntary movements may occur as well. A progressive cardiac involvement with repolarization disturbances, ventricular hypertrophy, and sinus-node dysfunction, ultimately leading to severe bradycardia and/or other conduction abnormalities, starts in the mid-teens. Patients are usually bedridden at 20 years of age, and death usually occurs in the third decade of life.

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幼年神经元样脂褐质病(巴滕病):目前的见解。
目前的综述主要集中在幼年神经元样脂褐质病(JNCL;由CLN3突变引起的巴顿病(Batten disease)。5-6岁左右出现的功能性视力障碍是80%以上患者的第一症状。大约2年后(尽管有时同时),出现明显的认知障碍迹象。行为问题可以提前发生,尤其是男孩。这些症状包括焦虑和抑郁情绪、攻击行为、幻觉,甚至精神病症状。在青少年之后,会出现严重的痴呆症,包括记忆力、注意力和一般推理能力的丧失,以及独立适应技能的丧失,比如行动能力、进食能力和沟通能力。睡眠异常,如解决问题,夜间醒来和噩梦,报告在一半以上的患者。绝大多数(如果不是全部)患者在大约10岁时开始发作。在大约一半的患者中,全身性强直-阵挛性发作是唯一的发作类型,在三分之一的患者中合并部分性发作。癫痫发作的严重程度似乎没有性别或基因型的差异,患者之间的癫痫发作活动有很大差异。诊断后不久,患者开始出现轻微的共济失调症状,青春期锥体外系症状(僵硬、运动迟缓、步伐缓慢伴髋膝屈曲)出现的频率越来越高。咀嚼和吞咽也会出现困难,在青少年晚期,食物摄入也会受到阻碍。也可能出现周期性的不自主运动。进行性心脏受累,伴复极障碍、心室肥厚和窦结功能障碍,最终导致严重心动过缓和/或其他传导异常,开始于青少年中期。患者通常在20岁时卧床不起,死亡通常发生在生命的第三个十年。
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