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Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-van Laere syndrome) with hyperintense brainstem nuclei on magnetic resonance imaging: new finding in three siblings.
Koul, Roshan; Jain, Rajeev; Chacko, Alexander; Alfutaisi, Amna; Hashim, Javad; Chacko, Jacob.
Afiliação
  • Koul R; Division of Paediatric Neurology, Department of Child Health, Sultan Qaboos University Hospital, PO Box 38, Al-Khod 123, Muscat, Sultanate of Oman. koul@squ.edu.om
J Child Neurol ; 21(6): 523-5, 2006 Jun.
Article em En | MEDLINE | ID: mdl-16948939
Three siblings (one boy and two girls) with Brown-Vialetto-van Laere syndrome are reported. A peculiar feature of onset with hearing loss in a patient with multiple cranial nerve palsies and a positive family history suggests this diagnosis. In our family, an autosomal recessive mode of inheritance was seen. In addition, we observed that early onset was associated with rapid deterioration and death. Optic nerve involvement and hyperintensity of the brainstem nuclei on magnetic resonance imaging (MRI) are two new features described in this report.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nervo Óptico / Paralisia Bulbar Progressiva / Tronco Encefálico / Perda Auditiva Neurossensorial Tipo de estudo: Diagnostic_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2006 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nervo Óptico / Paralisia Bulbar Progressiva / Tronco Encefálico / Perda Auditiva Neurossensorial Tipo de estudo: Diagnostic_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2006 Tipo de documento: Article