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亨廷顿舞蹈病。3例报告及文献复习

Huntington's chorea. Report of 3 cases and review of the literature.

作者信息

Osborne J P, Munson P, Burman D

出版信息

Arch Dis Child. 1982 Feb;57(2):99-103. doi: 10.1136/adc.57.2.99.

Abstract

Three cases of Huntington's chorea with onset before age 10 years are reported. Each child presented with rigidity and indistinct speech, and there was progressive deterioration. Necropsy examination confirmed the diagnosis in 2 of them. A review of reports showed a further 43 cases with onset before 10 years. The rigid variety of disease was seen most often, but isolated chorea and isolated progressive mental deterioration occurred. Fits were common but occurred late and were often difficult to control. Dysarthria was common and occurred early. The duration of illness was very variable and ranged from 2 to 38 years. Symptoms can occur in a child before appearing in the affected parent who is most likely to be the father. Affected siblings develop the disease early, often in the first decade. Siblings of patients with onset before age 10 years who are unaffected by age 25 years had only an 8% chance of developing the disease, compared with a 50% chance in unselected at risk individuals of the same age.

摘要

报告了3例10岁前发病的亨廷顿舞蹈症病例。每个患儿均表现为肌张力增高和言语不清,且病情呈进行性恶化。尸检确诊了其中2例。文献回顾显示另有43例10岁前发病的病例。最常见的是肌张力障碍型疾病,但也有孤立性舞蹈症和孤立性进行性精神衰退病例。癫痫发作很常见,但出现较晚且常难以控制。构音障碍常见且出现较早。病程差异很大,从2年到38年不等。症状可能在患儿身上先出现,然后才出现在最可能是父亲的患病父母身上。患病的兄弟姐妹发病较早,通常在第一个十年内。10岁前发病且到25岁时未患病的患者的兄弟姐妹患该病的几率仅为8%,而同龄未经过筛选的高危个体患该病的几率为50%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b94/1627539/7dab55ffea76/archdisch00761-0018-a.jpg

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