Literature DB >> 3655850

Juvenile-onset bulbospinal muscular atrophy with deafness: Vialetta-van Laere syndrome or Madras-type motor neuron disease?

B A Summers1, M Swash, M S Schwartz, D A Ingram.   

Abstract

A girl with rapid-onset, bulbospinal muscular atrophy and deafness is described. The patient's mother and brother showed EMG features consistent with subclinical involvement. T is bulbospinal form of spinal muscular atrophy associated with deafness described by Vialetto and van Laere closely resembles the Madras type of motor neuron disease, also associated with deafness, described by Jagganathan and colleagues.

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Year:  1987        PMID： 3655850     DOI： 10.1007/bf00314095

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


  8 in total

1.  Preservation of a certain motoneurone group of the sacral cord in amyotrophic lateral sclerosis: its clinical significance.

Authors:  T Mannen; M Iwata; Y Toyokura; K Nagashima
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-05       Impact factor: 10.154

2.  Clinical-anatomic study of a family with bulbo-spinal muscular atrophy in adults.

Authors:  D Schiffer; F Brignolio; A Chio; M T Giordana; A Migheli
Journal:  J Neurol Sci       Date:  1986-03       Impact factor: 3.181

3.  [Cochleovestibular data in amyotrophic lateral sclerosis (Van Laere's form)].

Authors:  C C Atherino Tavares; J Pitágoras de Mattos; A Coelho de Amorim
Journal:  Rev Laryngol Otol Rhinol (Bord)       Date:  1985

4.  Ponto-bulbar palsy with deafness (Brown-Vialetto-Van Laere syndrome).

Authors:  V Gallai; J M Hockaday; J T Hughes; D J Lane; D R Oppenheimer; G Rushworth
Journal:  J Neurol Sci       Date:  1981-05       Impact factor: 3.181

5.  [Familial progressive chronic bulbo-pontine paralysis with deafness. A case of Klippel-Trenaunay syndrome in siblings of the same family. Diagnostic and genetic problems].

Authors:  J Van Laere
Journal:  Rev Neurol (Paris)       Date:  1966-08       Impact factor: 2.607

6.  Anterior horn cell disease seen in South India.

Authors:  Z A Sayeed; C U Velmurugendran; G Arjundas; M Masarreen; K Valmikinathan
Journal:  J Neurol Sci       Date:  1975-12       Impact factor: 3.181

7.  [Charcot's disease and juvenile amyotrophic lateral sclerosis].

Authors:  M Ben Hamida; F Hentati
Journal:  Rev Neurol (Paris)       Date:  1984       Impact factor: 2.607

8.  Progressive bulbar paralysis associated with neural deafness. A nosological entity.

Authors:  R Alberca; C Montero; A Ibañez; D I Segura; G Miranda-Nieves
Journal:  Arch Neurol       Date:  1980-04
  8 in total
  5 in total

1.  A Case with Brown-Vialetto-Van Laere Syndrome: A Sudden Onset Auditory Neuropathy Spectrum Disorder.

Authors:  Başak Mutlu; Merve Torun Topçu; Ayça Çiprut
Journal:  Turk Arch Otorhinolaryngol       Date:  2019-12-01

2.  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 3.  Brown-Vialetto-Van Laere syndrome.

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

4.  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.  Madras motor neuron disease (MMND) is distinct from the riboflavin transporter genetic defects that cause Brown-Vialetto-Van Laere syndrome.

Authors:  Atchayaram Nalini; Amelie Pandraud; Kin Mok; Henry Houlden
Journal:  J Neurol Sci       Date:  2013-08-13       Impact factor: 3.181
  5 in total

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