Literature DB >> 24283576

Hereditary juvenile parkinsonism with pyramidal signs and mental retardation.

N P Quinn1, P J Goadsby, A J Lees.   

Abstract

We describe two patients who developed, in the first and second decades of life, mental retardation, some limitation of up gaze, poorly levodopa-responsive parkinsonism and pyramidal signs. Recessive inheritance is suggested by the fact that they were subsequently found to be first cousins from consanguineous unions. A number of different possible diagnoses were considered, but despite extensive investigation these patients, who are both still living, thus far appear to be unique. In particular, unlike most cases of alleged "pallido-pyramidal disease" in the literature, we do not feel it justifiable to use this denomination in the absence of either pathological or in vivo imaging evidence of pallidal involvement. 1995 Lippincott Williams & Wilkins.

Entities:  

Year:  1995        PMID: 24283576     DOI: 10.1111/j.1468-1331.1995.tb00088.x

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  2 in total

1.  Action Myoclonus and Seizure in Kufor-Rakeb Syndrome.

Authors:  Mohammad Rohani; Anthony E Lang; Farzad Sina; Elahe Elahi; Alfonso Fasano; John Hardy; Jose Bras; Afagh Alavi
Journal:  Mov Disord Clin Pract       Date:  2017-12-28

2.  Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.

Authors:  Coro Paisán-Ruiz; Rocio Guevara; Monica Federoff; Hasmet Hanagasi; Fardaz Sina; Elahe Elahi; Susanne A Schneider; Petra Schwingenschuh; Nin Bajaj; Murat Emre; Andrew B Singleton; John Hardy; Kailash P Bhatia; Sebastian Brandner; Andrew J Lees; Henry Houlden
Journal:  Mov Disord       Date:  2010-09-15       Impact factor: 10.338

  2 in total

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