Literature DB >> 1291912

[A case of progressive bulbar paralysis in a child (Fazio-Londe disease)].

W Drozdowski1, K Czerwińska-Ciechan, E Jankowicz, J Smigielska.   

Abstract

The reported case was diagnosed in a girl aged 14, in whom the first signs developed at the age of 6, with progressive involvement of the cranial nerves IX, X, XI and XII, and V with VII. After ruling out other possible causes the diagnosis of the Fazio-Londe disease was established. Electromyographic examination confirming the diagnosis demonstrated also evidence of changes of neurogenic type in the muscles of upper extremities despite absence of demonstrable clinical abnormalities, which, as suggest the authors, may support the hypothesis of the similarity of the disease to other forms of spinal muscular atrophy, such as Werdnig-Hoffman and Kugelberg-Welander diseases.

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Year:  1992        PMID: 1291912

Source DB:  PubMed          Journal:  Neurol Neurochir Pol        ISSN: 0028-3843            Impact factor:   1.621


  1 in total

1.  Progressive bulbur paralysis (Fazio-Londe disease).

Authors:  Taruna Gulati; Vivek Dewan; Praveen Kumar; Bina Ahuja; V K Anand
Journal:  Indian J Pediatr       Date:  2004-01       Impact factor: 1.967

  1 in total

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