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遗传性感觉神经病:常染色体显性类型的活检研究

Hereditary sensory neuropathy: biopsy study of an autosomal dominant variety.

作者信息

Danon M J, Carpenter S

出版信息

Neurology. 1985 Aug;35(8):1226-9. doi: 10.1212/wnl.35.8.1226.

Abstract

We studied sural nerve biopsies from a family in which three members in two generations (father, son, and daughter) had a dominantly inherited neuropathy (HSAN-I). There was marked loss of myelinated fibers, especially those of large diameter, and there was comparable loss of unmyelinated fibers. These quantitative findings differed from another reported case that provided basis for the classification of dominant and recessively inherited sensory neuropathies. Few patients have been studied, so ultrastructural and morphometric data have limited value in classification of these disorders, for which there is still no known biochemical marker.

摘要

我们研究了一个家族的腓肠神经活检样本,该家族两代人中的三名成员(父亲、儿子和女儿)患有显性遗传性神经病(遗传性感觉神经病I型)。有明显的有髓纤维丢失,尤其是那些大直径的纤维,并且无髓纤维也有类似程度的丢失。这些定量研究结果与另一例报告病例不同,后者为显性和隐性遗传性感觉神经病的分类提供了依据。研究的患者很少,因此超微结构和形态计量学数据在这些疾病的分类中价值有限,目前仍没有已知的生化标志物。

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