HaNDL Syndrome: A rare and overlooked disease
Authors : İlkin İyigündoğdu, Eda Derle
Pages : 112-114
View : 35 | Download : 63
Publication Date : 2025-07-28
Article Type : Other Papers
Abstract :Transient headache and neurological deficits with cerebrospinal fluid lymphocytosis (HaNDL) syndrome is a rare and misdiagnosed condition characterized with temporary neurological deficits, headache and pleocytosis in cerebrospinal fluid (CSF). Symptoms vary widely in patients and many neurological diseases such as stroke, migraine, encephalitis and epilepsy should be considered in the differential diagnosis. In this report, we described a 41-year-old female patient with HaNDL syndrome presenting with dysphasia and headache and we aimed to highlight the disease by discussing the clinical features, management and follow up period of the disease. It is important to raise awareness of its existence to avoid unnecessary and potentially harmful research and treatments.Keywords : HaNDL Sendromu, başağrısı, lenfositoz, psödomigren
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