Neuro-respiratory pathology in spinocerebellar ataxia

被引:2
|
作者
Biswas, Debolina D. [1 ]
El Haddad, Lea [1 ]
Sethi, Ronit [1 ]
Huston, Meredith L. [1 ]
Lai, Elias [1 ]
Abdelbarr, Mariam M. [1 ]
Mhandire, Doreen Z. [1 ]
ElMallah, Mai K. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Pediat, Div Pulm & Sleep Med, Box 2644, Durham, NC 27710 USA
关键词
Spinocerebellar ataxia; Medulla; Phrenic; Hypoglossal nerve; Respiratory failure; PRE-BOTZINGER COMPLEX; SPINAL-CORD DAMAGE; CAG REPEAT LENGTH; BRAIN-STEM; CLINICAL-FEATURES; SLEEP; DEGENERATION; INVOLVEMENT; TYPE-2; DYSFUNCTION;
D O I
10.1016/j.jns.2022.120493
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The spinocerebellar ataxias (SCA) are a heterogeneous group of neurodegenerative disorders with an autosomal dominant inheritance. Symptoms include poor coordination and balance, peripheral neuropathy, impaired vision, incontinence, respiratory insufficiency, dysphagia, and dysarthria. Although many patients with SCA have respiratory-related complications, the exact mechanism and extent of this pathology remain unclear. This review aims to provide an update on the recent clinical and preclinical scientific findings on neuropathology causing respiratory insufficiency in SCA.
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页数:9
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