Literature DB >> 17052005

[Amyotrophic lateral sclerosis associated with extrapyramidal symptoms or signs].

Kiwa Hama1, Tameko Kihira, Masae Okawa, Yoshinori Kajimoto, Yasuhiro Hiwatani, Shuhei Morita, Ichiro Nakanishi, Hideto Miwa, Tomoyoshi Kondo.   

Abstract

This investigation was conducted to clarify the frequency and characteristics of ALS associated with extrapyramidal symptoms or signs in Wakayama prefecture. The questionnaires to survey ALS cases were mailed to all medical centers in Wakayama prefecture. A total of 252 cases were found to have motor neuron diseases. Among them, 204 cases fulfilled probable or definite according to El Escorial Criteria. In 10 of them, extrapyramidal signs were identified as follows: rigidity 50%, tremor 40% and akinesia 10%. Family history of ALS in these cases (20%) is higher than expected in usual ALS, and all of them are negative for SOD-1 mutation. Dementia and autonomic nervous symptoms were observed in several cases. Incidence of extrapyramidal signs in ALS resulted in 4.8%. The incidence of extrapyramidal signs is more frequent than expected by chance, suggesting that the degeneration of basal ganglia and/or substantia nigra may not be so rare in ALS.

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Year:  2006        PMID: 17052005

Source DB:  PubMed          Journal:  No To Shinkei        ISSN: 0006-8969


  1 in total

1.  Tremor in X-linked recessive spinal and bulbar muscular atrophy (Kennedy's disease).

Authors:  Francisco A Dias; Renato P Munhoz; Salmo Raskin; Lineu César Werneck; Hélio A G Teive
Journal:  Clinics (Sao Paulo)       Date:  2011       Impact factor: 2.365

  1 in total

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