ntrk1相关的遗传性感觉和自主神经病变4型:组胺激发试验的作用

Child neurology open Pub Date : 2022-06-20 eCollection Date: 2022-01-01 DOI:10.1177/2329048X221108826
Amytice Mirchi, Julie Richer, Maryam Oskoui, Hugh J McMillan
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摘要

遗传性感觉和自主神经病变(HSAN)是一种罕见的以无髓神经纤维功能受损为特征的遗传遗传病。在这里,我们报告一个病人的自残行为和减少对疼痛的反应,暗示一个潜在的小纤维神经病变。神经传导检查正常,但左臂没有交感皮肤反应。皮内组胺激发试验评估小无髓神经纤维的功能,并发现没有耀斑反应。利用全基因组测序,在神经营养型酪氨酸激酶1型基因中发现了一种新的变异,扩大了已知的与HSAN 4型相关的致病变异。通过这个病例,我们证明了组胺激发试验在怀疑患有小纤维神经病变的患者中的作用,这些患者的电生理测试可能是正常的,并且可能出现非特异性症状,包括张力低下和发育不全。获得的信息可以指导基因检测,并有助于解释新发现的变异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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NTRK1-related Hereditary Sensory and Autonomic Neuropathy Type 4: The Role of the Histamine Challenge Test.

Hereditary sensory and autonomic neuropathies (HSAN) are rare, genetically inherited disorders characterized by impaired unmyelinated nerve fiber function. Here we report a patient with self-mutilation behavior and decreased response to pain, suggestive of an underlying small fiber neuropathy. Nerve conduction studies were normal but sympathetic skin response was absent at the left arm. Intradermal histamine challenge test was performed to evaluate the function of small unmyelinated nerve fibers and revealed absence of a flare response. Using whole genome sequencing, a novel variant in the neurotrophic tyrosine kinase type 1 gene was identified, expanding the known disease-causing variants associated with HSAN type 4. Through this case, we demonstrate the role of the histamine challenge test in patients suspected to have a small fiber neuropathy where electrophysiological testing may be normal and who may present with non-specific symptoms including hypotonia and failure to thrive. The information gained can guide genetic testing and contribute to interpretation of new variants identified.

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