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Strategy for genetic analysis in hereditary neuropathy.
Masingue, M; Fernández-Eulate, G; Debs, R; Tard, C; Labeyrie, C; Leonard-Louis, S; Dhaenens, C-M; Masson, M A; Latour, P; Stojkovic, T.
Afiliação
  • Masingue M; Centre de référence des maladies neuromusculaires Nord/Est/Île-de-France, hôpital Pitié-Salpêtrière, AP-HP, Paris, France. Electronic address: marion.masingue@aphp.fr.
  • Fernández-Eulate G; Centre de référence des maladies neuromusculaires Nord/Est/Île-de-France, hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Debs R; Service de neurophysiologie, hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Tard C; CHU de Lille, clinique neurologique, centre de référence des maladies neuromusculaires Nord/Est/Île-de-France, 59037 Lille cedex, France.
  • Labeyrie C; Service de neurologie, hôpital Kremlin-Bicêtre, AP-HP, Le Kremlin-Bicêtre, France.
  • Leonard-Louis S; Centre de référence des maladies neuromusculaires Nord/Est/Île-de-France, hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Dhaenens CM; Université de Lille, Inserm, CHU de Lille, U1172-LilNCog-Lille Neuroscience & Cognition, 59000 Lille, France.
  • Masson MA; Inserm U1127, Paris Brain Institute, ICM, Sorbonne Université, CNRS UMR 7225, hôpital Pitié-Salpêtrière, Paris, France.
  • Latour P; Service de biochimie biologie moléculaire, CHU de Lyon, centre de biologie et pathologie Est, 69677 Bron cedex, France.
  • Stojkovic T; Centre de référence des maladies neuromusculaires Nord/Est/Île-de-France, hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
Rev Neurol (Paris) ; 179(1-2): 10-29, 2023.
Article em En | MEDLINE | ID: mdl-36566124
Inherited neuropathies are a heterogeneous group of slowly progressive disorders affecting either motor, sensory, and/or autonomic nerves. Peripheral neuropathy may be the major component of a disease such as Charcot-Marie-Tooth disease or a feature of a more complex multisystemic disease involving the central nervous system and other organs. The goal of this review is to provide the clinical clues orientating the genetic diagnosis in a patient with inherited peripheral neuropathy. This review focuses on primary inherited neuropathies, amyloidosis, inherited metabolic diseases, while detailing clinical, neurophysiological and potential treatment of these diseases.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuropatia Hereditária Motora e Sensorial / Doença de Charcot-Marie-Tooth Limite: Humans Idioma: En Revista: Rev Neurol (Paris) Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuropatia Hereditária Motora e Sensorial / Doença de Charcot-Marie-Tooth Limite: Humans Idioma: En Revista: Rev Neurol (Paris) Ano de publicação: 2023 Tipo de documento: Article