Heim P, Claussen M, Hoffmann B, Conzelmann E, Gärtner J, Harzer K, Hunneman D H, Köhler W, Kurlemann G, Kohlschütter A
Department of Pediatrics, University of Hamburg, Germany.
Am J Med Genet. 1997 Sep 5;71(4):475-8.
Through a survey of all departments of pediatrics, neurology and neuropathology in Germany, we calculated the incidence of all major forms of leukodystrophy. Only diagnoses based on specific biochemical tests in association with typical findings and/or neuroradiologically proven white matter involvement were accepted. In accordance with these strict criteria, 617 cases of leukodystrophy were found (incidence of all forms: app. 2.0/100,000). Minimal incidence was estimated at 0.8/100,000 for adrenoleukodystrophy/adrenomyeloneuropathy (ALD/AMN), 0.6/100,000 for metachromatic leukodystrophy (MLD), and 0.6/100,000 for Krabbe disease. Thus ALD/AMN is apparently underdiagnosed in Germany. A considerable proportion of leukodystrophies could not be classified in spite of adequate diagnostic procedures in experienced centers.
通过对德国所有儿科、神经科和神经病理学部门进行调查,我们计算了所有主要形式脑白质营养不良的发病率。仅接受基于特定生化检测并伴有典型表现和/或经神经放射学证实的白质受累情况的诊断。根据这些严格标准,共发现617例脑白质营养不良病例(所有形式的发病率:约2.0/100,000)。肾上腺脑白质营养不良/肾上腺脊髓神经病(ALD/AMN)的最低发病率估计为0.8/100,000,异染性脑白质营养不良(MLD)为0.6/100,000,克拉伯病为0.6/100,000。因此,ALD/AMN在德国显然存在诊断不足的情况。尽管经验丰富的中心采用了适当的诊断程序,但仍有相当一部分脑白质营养不良无法分类。