神经学
医学
共济失调
离子通道病
肾病科
儿科
介绍(产科)
肾小管病变
肌张力障碍
内科学
精神科
肾脏疾病
外科
作者
Pedro Henrique Almeida Fraiman,Thiago Yoshinaga Tonholo Silva,Breno Kazuo Massuyama,Luíza Alves Corazza,Luane Abdalla Gouvea,Ivana Rocha Raslan,Orlando Graziani Póvoas Barsottini,José Luiz Pedroso
标识
DOI:10.1136/pn-2025-004565
摘要
A 32-year-old woman had experienced recurrent seizures since infancy, with progressive ataxia, dystonia, and electrolyte disturbances, suggesting a possible genetic tubulopathy with neurological manifestations. The complexity of her presentation highlights the importance of a multidisciplinary approach and the role of genetic investigations in uncovering rare conditions that bridge neurology and nephrology.
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