Literature DB >> 18539998

Vanishing white matter disease: the first reported chinese patient.

Sheila S N Wong1, David C K Luk, Virginia C N Wong, Gert C Scheper, Marjo S van der Knaap.   

Abstract

Vanishing white matter disease is a rare neurological disease. The majority of patients reported are Caucasian individuals. We describe the first Chinese patient with typical clinical and radiological features genetically confirmed to have vanishing white matter disease for a mutation in EIF2B4, followed by a brief review of the disease.

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Year:  2008        PMID: 18539998     DOI: 10.1177/0883073808314154

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  1 in total

1.  Vanishing white matter disease with mutations in EIF2B5 gene.

Authors:  Suvasini Sharma; Mohemmed Ajij; Varinder Singh; Satinder Aneja
Journal:  Indian J Pediatr       Date:  2014-09-18       Impact factor: 1.967

  1 in total

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