Frontal ataksi: Ataksi spektrumunda sık görülen ancak az tanınan bir bozukluktur.

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BackgroundAtaxia comprises a heterogeneous group of disorders with multiple clinical and etiological presentations. The frontal subtype, in particular, is poorly defined and often misdiagnosed, reflecting both its complex historical evolution and lack of formal diagnostic criteria.ObjectiveTo evaluate clinical and epidemiological characteristics of a sample of patients with ataxia under follow-up in a private neurology clinic.MethodsWe evaluated 48 patients diagnosed with ataxia over a 4-month period and followed them for 1-year in a private neurology clinic in southern Brazil. Clinical, neuroimaging, and laboratory data were analyzed. Patients were classified according to clinical and etiological subtypes based on criteria defined by the authors.ResultsFrontal ataxia was the most frequent presentation (n = 15; 31.3%), predominantly affecting elderly patients with systemic arterial hypertension, diabetes mellitus, and MRI evidence of small vessel disease. These patients had a later disease onset (mean: 75.9 ± 8.8 years), lower SARA scores, and a nonprogressive course compared with degenerative cerebellar ataxias (p p = 0.31). Hereditary ataxias, particularly spinocerebellar ataxias (SCAs), were the second most frequent group, followed by atypical Parkinsonian syndromes.ConclusionFrontal ataxia emerged as a frequent and underrecognized subtype in routine neurological practice. These findings underscore the need for increased awareness and the development of evidence-based diagnostic criteria to better define and distinguish it within the spectrum of ataxic disorders.

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