Literature DB >> 11601179

[Kennedy disease in a patient with progressive speech disorder].

J Kárteszi1, E Morava, M Czakó, I Gáti, J Czopf, G Kosztolányi, B Melegh.   

Abstract

Kennedy disease is an adult onset neuromuscular disease characterized by slowly progressive proximal and bulbar muscle weakness. The disease associates with gynecomastia, adult onset infertility and sensory neuropathy, and caused by pathologic expansion of CAG repeats at the N-terminal region of the androgen-receptor gene at Xq11-q12. We report on a patient presenting with slowly progressive muscle weakness of the lower extremities, progressive dysartry and swallowing difficulties. The clinical symptoms were not fully specific for the disease. Moreover the family history was suggestive for an autosomal dominant trait meaning a diagnostic pitfall at the original examination. Finally the firm diagnosis of the Kennedy disease was established by a polimerase chain reaction based method.

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Year:  2001        PMID: 11601179

Source DB:  PubMed          Journal:  Orv Hetil        ISSN: 0030-6002            Impact factor:   0.540


  2 in total

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Authors:  Josef Finsterer; Claudia Stöllberger
Journal:  Mol Genet Metab Rep       Date:  2017-12-21

2.  Only some patients with bulbar and spinal muscular atrophy may develop cardiac disease.

Authors:  Josef Finsterer; Claudia Stöllberger
Journal:  Mol Genet Metab Rep       Date:  2017-11-06
  2 in total

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