Yonsei Medical Journal · 2014 · 15 citations · 10 references
MedicineMolecular GeneticsNeurologyMolecular NeuroscienceNeurogeneticsNeuropathologyCerebellar AnatomyHereditary NeuropathiesNeurogenetic DisordersWhite Matter DisordersCerebellar DiseaseCerebellar DysfunctionCerebellar ImagingCerebellar White MatterDentate NucleusDifferential Symptom DiagnosisWhite Matter LesionsX-linked Adrenoleukodystrophy
X-linked adrenoleukodystrophy (X-ALD) shows a wide range of phenotypic expression, but clinical presentation as an isolated lesion of the cerebellar white matter and dentate nuclei has not been reported. We report an unusual presentation of X-ALD only with an isolated lesion of the cerebellar white matter and dentate nuclei. The proband, a 37-year-old man presented with bladder incontinence, slurred speech, dysmetria in all limbs, difficulties in balancing, and gait ataxia. Brain magnetic resonance imaging showed an isolated signal change of white matter around the dentate nucleus in cerebellum. With high level of very long chain fatty acid, gene study showed a de novo mutation in exon 1 at nucleotide position c.277_296dup20 (p.Ala100Cysfs*10) of the adenosine triphosphate-binding cassette D1 gene. It is advised to consider X-ALD as a differential diagnosis in patients with isolated cerebellar degeneration symptoms.
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Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy
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Natural history of X-linked adrenoleukodystrophy in Japan
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MRI of adrenoleukodystrophy involving predominantly the cerebellum and brain stem
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X‐linked adrenoleukodystrophy with olivopontocerebellar atrophy
Marika Vianello, Renzo Manara, Corrado Betterle et al. · European Journal of Neurology · 2005 · 22 citations
Medicine, Neurology, Neuroscience +17