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Volumn 8, Issue 3, 2013, Pages 257-259

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

Author keywords

[No Author keywords available]

Indexed keywords

AUDITORY STIMULATION; BROWN VIALETTO VAN LAERE SYNDROME; CASE REPORT; CEREBRAL PALSY; CHILD; DYSARTHRIA; DYSPHAGIA; DYSPHONIA; ELECTROMYOGRAPHY; EVOKED BRAIN STEM AUDITORY RESPONSE; FEMALE; HUMAN; LETTER; PERCEPTION DEAFNESS; PONTOBULBAR PALSY; SCHOOL CHILD; WEAKNESS;

EID: 84891952082     PISSN: 18171745     EISSN: 19983948     Source Type: Journal    
DOI: 10.4103/1817-1745.123709     Document Type: Letter
Times cited : (2)

References (10)
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  • 2
    • 77949273807 scopus 로고    scopus 로고
    • Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54
    • Green P, Wiseman M, Crow YJ, Houlden H, Riphagen S, Lin JP, et al. Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54. Am J Hum Genet 2010;86:485-9.
    • (2010) Am J Hum Genet , vol.86 , pp. 485-489
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  • 3
    • 0342314442 scopus 로고    scopus 로고
    • Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance?
    • Mégarbané A, Desguerres I, Rizkallah E, Delague V, Nabbout R, Barois A, et al. Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance? Am J Med Genet 2000;92:117-21.
    • (2000) Am J Med Genet , vol.92 , pp. 117-121
    • Mégarbané, A.1    Desguerres, I.2    Rizkallah, E.3    Delague, V.4    Nabbout, R.5    Barois, A.6
  • 4
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    • Four cases of Brown-Vialetto-van Laere syndrome from Iran: Clinical and electrophysiologic findings
    • Yadegari S, Dezfouli MA, Nafissi S, Ghorbani A. Four cases of Brown-Vialetto-van Laere syndrome from Iran: Clinical and electrophysiologic findings. Iran J Neurol 2011;10: 54-7.
    • (2011) Iran J Neurol , vol.10 , pp. 54-57
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  • 6
    • 0023390542 scopus 로고
    • Juvenile-onset bulbospinal muscular atrophy with deafness: Vialetta-van Laere syndrome or Madras-type motor neuron disease?
    • Summers BA, Swash M, Schwartz MS, Ingram DA. Juvenile-onset bulbospinal muscular atrophy with deafness: Vialetta-van Laere syndrome or Madras-type motor neuron disease? J Neurol 1987;234:440-2.
    • (1987) J Neurol , vol.234 , pp. 440-442
    • Summers, B.A.1    Swash, M.2    Schwartz, M.S.3    Ingram, D.A.4
  • 9
    • 0024509068 scopus 로고
    • Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: A dominant form of spinal muscular atrophy?
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    • (1989) J Med Genet , vol.26 , pp. 105-108
    • Boltshauser, E.1    Lang, W.2    Spillmann, T.3    Hof, E.4
  • 10
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    • Clinical pattern of motor neuron disease seen in younger age groups in Madras
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.