Article Text
Neurological rarity
An unusual gait following the discovery of a new disease
Abstract
A 39-year-old woman presented to the neurology clinic with an abnormal gait. Subsequent investigations confirmed a rare neurodegenerative disease. This case highlights the key clinical features and diagnostic approach to neuroferritinopathy, and describes the discovery of the disease in a family from Cumbria in the north west of England.
Statistics from Altmetric.com
Footnotes
Competing interests None.
Patient consent Obtained.
Provenance and peer review Commissioned; not externally peer reviewed.
Read the full text or download the PDF:
Other content recommended for you
- The Bare Essentials
- The differential diagnosis of Huntington's disease-like syndromes: ‘red flags’ for the clinician
- Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum
- The differential diagnosis of chorea
- Late adult onset chorea with typical pathology of Hallervorden-Spatz syndrome
- Parkinson's disease: chameleons and mimics
- Clinical and genetic delineation of neurodegeneration with brain iron accumulation
- Neurological disorders presenting mainly in adolescence
- Chorea and related disorders
- Neuroferritinopathy in a French family with late onset dominant dystonia