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Mendenhalls syndrome: clues to the aetiology of human diabetic neuropathy.

机译:Mendenhall综合征:人类糖尿病性神经病的病因线索。

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摘要

The pathogenesis of human diabetic neuropathy remains unclear. Mendenhall's syndrome is characterised by a mutation in the insulin receptor gene with consequent lifelong uncontrolled hyperglycaemia. The sural nerve biopsy from a patient with Mendenhall's syndrome showed a gross loss of myelinated fibres that was comparable with the degree of fibre loss in a case matched diabetic patient with established neuropathy. The biopsy from the patient with Mendenhall's syndrome showed only a very mild degree of microangiopathy, however, which failed to relate to the degree of nerve fibre loss and also did not compare with the advanced degree of microangiopathy seen in the diabetic patient. Thus hyperglycaemia itself did not result in appreciable microangiopathy. Furthermore the presence of severe neuropathy without advanced microangiopathy suggests an important and independent role for metabolic factors in the pathogenesis of neuropathy.
机译:人类糖尿病性神经病的发病机制仍不清楚。 Mendenhall综合征的特征是胰岛素受体基因发生突变,从而导致终生无法控制的高血糖症。 Mendenhall综合征患者的腓肠神经活检显示,髓鞘纤维的总体损失与在患有神经病的糖尿病患者中的纤维损失程度相当。 Mendenhall综合征患者的活检仅显示了非常轻度的微血管病变,但是,这与神经纤维丢失的程度没有关系,也没有与糖尿病患者所见的晚期微血管病变的程度进行比较。因此,高血糖症本身并未导致明显的微血管病变。此外,没有晚期微血管病变的严重神经病变的存在表明代谢因子在神经病变的发病机理中具有重要且独立的作用。

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