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A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus-Merzbacher disease: A new MRI finding.
Pavlidou, Efterpi; Ramachandran, Vijaya; Govender, Veronica; Wilson, Clare; Das, Rini; Vlachou, Victoria; Pavlou, Evangelos; Saggar, Anand; Mankad, Kshitij; Kinali, Maria.
Afiliação
  • Pavlidou E; Department of Paediatric Neurology, Chelsea and Westminster NHS Foundation Trust, London, United Kingdom.
  • Ramachandran V; South West Thames Regional Genetics Laboratory, St George's Hospital, NHS Foundation Trust, London, United Kingdom.
  • Govender V; Department of Paediatric Neurology, Chelsea and Westminster NHS Foundation Trust, London, United Kingdom.
  • Wilson C; Department of Paediatric Ophthalmology, Chelsea and Westminster NHS Foundation Trust, London, United Kingdom.
  • Das R; Department of Paediatric Neurology, Chelsea and Westminster NHS Foundation Trust, London, United Kingdom.
  • Vlachou V; Department of Paediatric Neurology, Chelsea and Westminster NHS Foundation Trust, London, United Kingdom.
  • Pavlou E; Department of Paediatric Neurology, 2nd Paediatric Department, A.H.E.P.A Hospital, Aristotle University of Thessaloniki, Greece.
  • Saggar A; South West Thames Regional Genetics Laboratory, St George's Hospital, NHS Foundation Trust, London, United Kingdom.
  • Mankad K; Department of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
  • Kinali M; Department of Paediatric Neurology, Chelsea and Westminster NHS Foundation Trust, London, United Kingdom. Electronic address: m.kinali@imperial.ac.uk.
Brain Dev ; 39(3): 271-274, 2017 Mar.
Article em En | MEDLINE | ID: mdl-27793435
ABSTRACT
Pelizaeus-Merzbacher disease (PMD) is a rare, X-linked disorder characterized by hypomyelination of the Central Nervous System due to mutations in the PLP1 gene. Certain mutations of the PLP1 gene correlate with specific clinical phenotypes and neuroimaging findings. We herein report a novel mutation of the PLP1 gene in two siblings with PMD associated with a rare and protean neuroimaging finding of optic nerve enlargement. To the best of our knowledge this is the first time that this novel mutation H133P of PLP1 gene is identified and clinically associated with optic nerve enlargement in PMD patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nervo Óptico / Imageamento por Ressonância Magnética / Proteína Proteolipídica de Mielina / Doença de Pelizaeus-Merzbacher / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nervo Óptico / Imageamento por Ressonância Magnética / Proteína Proteolipídica de Mielina / Doença de Pelizaeus-Merzbacher / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article