Literature DB >> 11465021

Brown-Vialetto-Van Laere syndrome: case report and literature review.

S Sathasivam1, S O'Sullivan, A Nicolson, P J Tilley, P J Shaw.   

Abstract

We describe a case of the Brown-Vialetto-Van Laere syndrome, which is a rare disorder characterized by progressive pontobulbar palsy associated with sensorineural deafness. More than 30 cases have been reported since the first case was described in 1894. We review the literature of this condition, comparing our case with those reported in the literature and emphasizing important features to improve our understanding of this syndrome.

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Year:  2000        PMID: 11465021     DOI: 10.1080/14660820050515106

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord        ISSN: 1466-0822


  5 in total

1.  Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings.

Authors:  Samira Yadegari; Askar Ghorbani; Mitra Ansari Dezfouli; Shahriar Nafissi
Journal:  Iran J Neurol       Date:  2011

Review 2.  Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy.

Authors:  Hooi Ling Teoh; Kate Carey; Hugo Sampaio; David Mowat; Tony Roscioli; Michelle Farrar
Journal:  Neural Plast       Date:  2017-05-28       Impact factor: 3.599

Review 3.  The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives.

Authors:  Annet M Bosch; Kevin Stroek; Nico G Abeling; Hans R Waterham; Lodewijk Ijlst; Ronald J A Wanders
Journal:  Orphanet J Rare Dis       Date:  2012-10-29       Impact factor: 4.123

Review 4.  Brown-Vialetto-Van Laere syndrome.

Authors:  Sivakumar Sathasivam
Journal:  Orphanet J Rare Dis       Date:  2008-04-17       Impact factor: 4.123

5.  Pontobulbar palsy and sensorineural deafness (Brown-Vialetto-van Laere syndrome): A case from Northwest Iran.

Authors:  Vahideh Toopchizadeh; Masood Ghahvechi Akbari; Afshin Habibzadeh
Journal:  J Pediatr Neurosci       Date:  2013-09
  5 in total

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