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[家族性自主神经功能异常的诊断与误诊]

[Diagnosis and misdiagnosis in familial dysautonomia].

作者信息

Maayan C, Kaplan E, Harrari M, Peleg O, Goldberg A

机构信息

Pediatric Dept., Hadassah-University Hospital, Mount Scopus, Jerusalem.

出版信息

Harefuah. 1994 May 15;126(10):565-7, 628.

PMID:8034241
Abstract

The method of diagnosis in 122 patients with familial dysautonomia (FD) was reviewed. In all cases the diagnosis was based on the clinical history, physical examination and results of the histamine test (concentrations of 1:1,000 and 1:10,000). In 8 patients the diagnosis was also supported by a meiotic response to pilocarpine (0.0625 mg/dl). 69 (56%) were diagnosed in the first year of life (19 of them relatives of known FD patients), 16 (13%) in the second year, 31 (25%) from 25 months to 10 years, 3 (2%) from 10.1-20 years, and 3 from 20.1-44 years. At diagnosis the mean age was 2.9 years (SD 5.84) and the median age 11 months. In 17 diagnosis was delayed by an average of 18.5 months (SD 16.9) from the time FD was initially suspected, mainly because of false interpretation of the histamine test. Early correct diagnosis is essential to prevent unnecessary morbidity and mortality from FD.

摘要

回顾了122例家族性自主神经功能异常(FD)患者的诊断方法。所有病例的诊断均基于临床病史、体格检查以及组胺试验结果(1:1000和1:10000浓度)。8例患者的诊断还得到了对毛果芸香碱(0.0625mg/dl)减数反应的支持。69例(56%)在出生后第一年确诊(其中19例是已知FD患者的亲属),16例(13%)在第二年确诊,31例(25%)在25个月至10岁确诊,3例(2%)在10.1至20岁确诊,3例在20.1至44岁确诊。确诊时的平均年龄为2.9岁(标准差5.84),中位年龄为11个月。17例患者从最初怀疑为FD到确诊平均延迟了18.5个月(标准差16.9),主要原因是对组胺试验的错误解读。早期正确诊断对于预防FD导致的不必要发病和死亡至关重要。

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