Natural History of SURF1 Deficiency: A Retrospective Chart Review

Pediatric Neurology(2023)

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摘要
The most common clinical symptoms were motor delay, verbal delay, intellectual and learning disability, dysphagia, feeding difficulties, and reflux. Neurological presentations include ataxia, hypotonia, visual/ocular abnormalities, dystonia, and imaging abnormalities include basal ganglia and brainstem lesions. Although heterogeneous, SURF1 deficiency should be considered with these clinical and imaging presentations and may support earlier identification.
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关键词
Charcot-Marie-Tooth disease 4K,Leigh syndrome,Mitochondrial disease,SURF1,SURF1 deficiency
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