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周期性呕吐综合征附加症

Cyclic vomiting syndrome plus.

作者信息

Boles Richard G, Powers Amy L R, Adams Kathleen

机构信息

Division of Medical Genetics, Childrens Hospital Los Angeles, Los Angeles, CA 90027, USA.

出版信息

J Child Neurol. 2006 Mar;21(3):182-8. doi: 10.2310/7010.2006.00040.

Abstract

Cyclic vomiting syndrome, which is characterized by severe discrete episodes of nausea, vomiting, and lethargy, is a fairly common, disabling, predominately childhood condition. Approximately 25% of cases have coexisting neuromuscular disease manifestations (cyclic vomiting syndrome plus). To determine whether patients with cyclic vomiting syndrome and neuromuscular disease represent a distinct subentity within cyclic vomiting syndrome, a clinical interview was conducted regarding 80 randomly ascertained sufferers of cyclic vomiting syndrome from a disease association database. Cyclic vomiting syndrome plus and "cyclic vomiting syndrome minus," herein defined as the presence of at least two and zero neuromuscular disease manifestations, were present in 23 and 44 subjects, respectively. Neuromuscular disease manifestations, including cognitive disorders, skeletal myopathy, cranial nerve dysfunction, and seizure disorders, were found to statistically cluster together among the same subjects. In addition, subjects with cyclic vomiting syndrome with neuromuscular disease had an earlier age at onset for vomiting episodes and a three- to eightfold statistically increased prevalence for certain dysautonomia-related (migraine, chronic fatigue, neurovascular dystrophy) and constitutional (growth retardation and birth defects) disorders. However, subjects with cyclic vomiting syndrome with and without neuromuscular disease were equally likely to have a sibling affected with neuromuscular disease manifestations. We conclude that cyclic vomiting syndrome plus, although likely not genetically distinct from cyclic vomiting syndrome minus, represents a distinct phenotypic entity that predicts an earlier onset of disease and increased comorbidity with a distinct list of medical conditions, possibly owing to a higher degree of mitochondrial dysfunction.

摘要

周期性呕吐综合征以严重的恶心、呕吐和嗜睡发作间断出现为特征,是一种相当常见、使人衰弱且主要发生于儿童期的病症。约25%的病例伴有神经肌肉疾病表现(周期性呕吐综合征伴发症)。为了确定周期性呕吐综合征伴神经肌肉疾病的患者是否代表周期性呕吐综合征中的一个独特亚组,我们从一个疾病关联数据库中随机选取了80名周期性呕吐综合征患者进行临床访谈。分别有23名和44名受试者存在周期性呕吐综合征伴发症和“周期性呕吐综合征无伴发症”(此处定义为存在至少两种和零种神经肌肉疾病表现)。在同一受试者中,神经肌肉疾病表现,包括认知障碍、骨骼肌病、颅神经功能障碍和癫痫发作疾病,在统计学上呈聚集状态。此外,患有周期性呕吐综合征伴神经肌肉疾病的受试者呕吐发作的起病年龄更早,某些自主神经功能障碍相关(偏头痛、慢性疲劳、神经血管营养不良)和体质性(生长发育迟缓及出生缺陷)疾病的患病率在统计学上增加了三至八倍。然而,患有和未患有神经肌肉疾病的周期性呕吐综合征受试者有患神经肌肉疾病表现的同胞的可能性相同。我们得出结论,周期性呕吐综合征伴发症虽然可能在基因上与周期性呕吐综合征无伴发症并无差异,但代表了一个独特的表型实体,它预示着疾病起病更早,且与一系列特定的病症共病率增加,这可能是由于线粒体功能障碍程度较高所致。

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