Allgrove (aaa)综合征的神经生理特征:病例报告及文献复习。

Child neurology open Pub Date : 2021-10-04 eCollection Date: 2021-01-01 DOI:10.1177/2329048X211031059
Daniel I Weiman, Meredith K Gillespie, Taila Hartley, Matthew Osmond, Yoko Ito, Kym M Boycott, Kristin D Kernohan, Matthew Lines, Hugh J McMillan
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引用次数: 0

摘要

Allgrove综合征或“aaa”综合征的特征是泪斑、失弛缓、促肾上腺皮质激素抵抗性肾上腺功能不全,以及中枢和周围神经系统受累。患者在出现症状的年龄、疾病严重程度和临床症状的性质方面表现出异质性。神经生理学测试也显示了变异性,包括:运动神经元疾病伴明显的球受累,运动为主的神经病变,或感觉运动多神经病变伴轴突或混合轴突和脱髓鞘特征。我们报告一个11岁的男孩谁提出了神经症状进行性痉挛和周围神经病变。他的神经生理检查证实为感觉运动多发性神经病,伴有轴突和脱髓鞘特征。外显子组测序鉴定出AAAS基因的复合杂合子变异。我们总结了他和其他29例Allgrove综合征患者的神经生理学结果,这些患者的神经传导研究结果是可用的,从而对这种罕见疾病中已报道的神经生理学结果的异质性进行了回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neurophysiological Characteristics of Allgrove (Triple A) Syndrome: Case Report and Literature Review.

Neurophysiological Characteristics of Allgrove (Triple A) Syndrome: Case Report and Literature Review.

Neurophysiological Characteristics of Allgrove (Triple A) Syndrome: Case Report and Literature Review.

Allgrove or "Triple A" syndrome is characterized by alacrima, achalasia, and adrenocorticotropic hormone-resistant adrenal insufficiency, as well as central and peripheral nervous system involvement. Patients demonstrate heterogeneity with regard to their age of symptom onset, disease severity, and nature of clinical symptoms. Neurophysiological testing has also shown variability ranging from: motor neuron disease with prominent bulbar involvement, motor-predominant neuropathy, or sensorimotor polyneuropathy with axonal or mixed axonal and demyelinating features. We report an 11-year-old boy who presented with neurological symptoms of progressive spasticity and peripheral neuropathy. His neurophysiological testing confirmed a sensorimotor polyneuropathy with axonal and demyelinating features. Exome sequencing identified compound heterozygote variants in the AAAS gene. We summarize the neurophysiological findings in him and 29 other patients with Allgrove syndrome where nerve conduction study findings were available thereby providing a review of the heterogeneity in neurophysiological findings that have been reported in this rare disorder.

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