Literature DB >> 6685241

Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs.

H R Jones, E T Hedley-Whyte.   

Abstract

Idiopathic hemochromatosis (IHC) is a genetically determined impairment in control of iron absorption that results in excessive parenchymal iron deposition, particularly in the liver. Of patients with IHC, 50% have little or no chemical evidence of liver dysfunction. Cirrhosis may be clinically occult, but still cause a syndrome of chronic hepatocerebral degeneration. Two patients are reported with IHC and a syndrome of ataxia, rigidity, myoclonic jerks, and dementia. Other associated symptoms may include diminished libido, decreased hearing, peripheral neuropathy, and large joint disease. Because symptoms of IHC can be reversed by phlebotomy, appropriate laboratory studies should be considered to exclude IHC in any patient with unexplained dementia, encephalopathy, and gait ataxia.

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Year:  1983        PMID: 6685241     DOI: 10.1212/wnl.33.11.1479

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  7 in total

1.  Hereditary hemochromatosis and movement disorders: the still controversial relationship. Response to Russo et al. in J Neurol (2004) 251:849-852.

Authors:  G Demarquay; S Thobois; P Latour; Emmanuel Broussolle
Journal:  J Neurol       Date:  2005-08-17       Impact factor: 4.849

2.  Chronic cerebellar ataxia and hereditary hemochromatosis: causal or coincidental association?

Authors:  M P Rutgers; A Pielen; M Gille
Journal:  J Neurol       Date:  2007-04-21       Impact factor: 4.849

3.  A parkinsonian movement disorder with brain iron deposition and a haemochromatosis mutation.

Authors:  Stefan Williams; Maruthi Ravi Vinjam; Azzam Ismail; Ahamad Hassan
Journal:  J Neurol       Date:  2013-06-23       Impact factor: 4.849

4.  Neuromuscular manifestations in hereditary haemochromatosis.

Authors:  S F Wouthuis; C Th B M van Deursen; M P te Lintelo; C A M Rozeman; R Beekman
Journal:  J Neurol       Date:  2010-04-01       Impact factor: 4.849

Review 5.  Overview of hemochromatosis.

Authors:  L H Smith
Journal:  West J Med       Date:  1990-09

Review 6.  Hereditary haemochromatosis is unlikely to cause movement disorders--a critical review.

Authors:  Noemi Russo; Mark Edwards; Thomasin Andrews; Michael O'Brien; Kailash P Bhatia
Journal:  J Neurol       Date:  2004-07       Impact factor: 4.849

7.  Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome.

Authors:  J E Nielsen; L N Jensen; K Krabbe
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-09       Impact factor: 10.154

  7 in total

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