Hereditary neuroferritinopathy presenting with palatal tremor, orofacial dyskinesias, bulbar symptoms, and unsteadiness of gait

Movement Disorders

Volumn 18, Issue 9, 2003, Pages 1057-

  Wills, Adrian ^a  

^a QUEEN S MEDICAL CENTRE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; FERRITIN; IRON;

ADULT; APRAXIA; BULBAR PARALYSIS; CASE REPORT; CLINICAL FEATURE; COGNITIVE DEFECT; DEGENERATIVE DISEASE; DYSARTHRIA; DYSPHAGIA; DYSTONIA; EDITORIAL; FRONTAL LOBE; GAIT DISORDER; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; HYPERKINESIA; MALE; MOTOR DYSFUNCTION; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; OROFACIAL DYSKINESIA; PALATE DISEASE; PHENOTYPE; PRIORITY JOURNAL; REFLEX DISORDER; SYMPTOMATOLOGY; TREMOR;

EID: 0141502263     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/mds.10496     Document Type: Editorial

References (2)

1. Curtis AR, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A, Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J. Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. Nat Genet 2001;28:350-354.
2. Wills AJ, Sawle GV, Guilbert PR, Curtis AR. Palatal tremor and cognitive decline in neuroferritinopathy. J Neurol Neurosurg Psychiatry 2002;73:91-92.