Neuro‐Behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (PAD) case report

Clinical Case Reports

Gholam Adeli¹  Abeer Sabry Safan¹  Mohammed Abunaib¹  Ahmed El Sotouhy²  Ahmed EL Beltagi²  Lina Yagan³ 

[1] Department of Neurology Neurosciences Institute Hamad Medical Corporation Doha Qatar;Department of Neuroradiology Neurosciences Institute Hamad Medical Corporation Doha Qatar;Weill Cornell Medicine of Cornell University (WCMCQ) Doha Qatar;

关键词: ataxia;    dysarthria;    midbrain lesion;    neuro‐Behçet's disease (NBD);    paroxysmal;   

DOI  :  10.1002/ccr3.5626

来源: DOAJ

【 摘 要 】

Abstract Paroxysmal dysarthria and ataxia (PDA) is a rare neurological manifestation of stereotyped attacks of sudden ataxic symptoms lasts for few seconds to minutes. We report a case of PDA in a 61‐year‐old male with a solitary homogenously enhancing solitary midbrain lesion and positive HLA‐B51 (Allele 2), controlled with lacosamide.

【 授权许可】

Unknown