Literature DB >> 24906253

Parkinsonism and inborn errors of metabolism.

A Garcia-Cazorla1, S T Duarte.   

Abstract

Parkinsonism is a frequent neurological syndrome in adulthood but is very rare in childhood. Early forms of Parkinsonism have many distinctive features as compared to Parkinsonism in adults. In fact, rather than Parkinsonism, the general concept "hypokinetic-rigid syndrome" (HRS) is more accurate in children. In general, the terms "dystonia-parkinsonism", "parkinsonism-plus", or "parkinsonism-like" are preferred to designate these forms of paediatric HRS. Inborn errors of metabolism (IEM) constitute an important group amongst the genetic causes of Parkinsonism at any age. The main IEM causing Parkinsonism are metal-storage diseases, neurotransmitter defects, lysosomal storage disorders and energy metabolism defects. IEM should not be neglected as many of them represent treatable causes of Parkinsonism. Here we review IEMs causing this neurological syndrome and propose diagnostic approaches depending on the age of onset and the associated clinical and neuroimaging features.

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Year:  2014        PMID: 24906253     DOI: 10.1007/s10545-014-9723-6

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  92 in total

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6.  Long-term benefit to pallidal deep brain stimulation in a case of dystonia secondary to pantothenate kinase-associated neurodegeneration.

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7.  Course in Parkinson disease subtypes: A 39-year clinicopathologic study.

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Journal:  Neurology       Date:  2009-07-21       Impact factor: 9.910

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9.  Recurrent collateral connections of striatal medium spiny neurons are disrupted in models of Parkinson's disease.

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Journal:  J Neurosci       Date:  2008-05-21       Impact factor: 6.167

10.  Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy.

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Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-08       Impact factor: 10.154

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