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Family with Ehlers-Danlos syndrome (combined classic and vascular type) with rare presentation of progressive myopathy and unusual association of severe facial and trigeminal motor weakness.
Nalini, A; Devaraddi, N; Gayathri, N; Prasad, Chandrajit; Preethish-Kumar, V; Polavarapu, K; Shantanu, S.
Afiliação
  • Nalini A; Department of Neurology, National Institute of Mental Health and Neuro Sciences, Bengaluru, Karnataka, India.
  • Devaraddi N; Department of Neurology, National Institute of Mental Health and Neuro Sciences, Bengaluru, Karnataka, India.
  • Gayathri N; Department of Neuropathology, National Institute of Mental Health and Neuro Sciences, Bengaluru, Karnataka, India.
  • Prasad C; Department of Neuro Imaging and Interventional Radiology, National Institute of Mental Health and Neuro Sciences, Bengaluru, Karnataka, India.
  • Preethish-Kumar V; Department of Clinical Neurosciences, National Institute of Mental Health and Neuro Sciences, Bengaluru, Karnataka, India.
  • Polavarapu K; Department of Clinical Neurosciences, National Institute of Mental Health and Neuro Sciences, Bengaluru, Karnataka, India.
  • Shantanu S; Department of Neurology, National Institute of Mental Health and Neuro Sciences, Bengaluru, Karnataka, India.
Neurol India ; 65(3): 561-565, 2017.
Article em En | MEDLINE | ID: mdl-28488622
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saúde da Família / Músculo Esquelético / Debilidade Muscular / Síndrome de Ehlers-Danlos Tipo de estudo: Risk_factors_studies Limite: Adolescent / Adult / Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saúde da Família / Músculo Esquelético / Debilidade Muscular / Síndrome de Ehlers-Danlos Tipo de estudo: Risk_factors_studies Limite: Adolescent / Adult / Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article