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Roussy-Lévy Syndrome: Pes Cavus, Tendon Areflexia, Amyotrophy, Gait Ataxia, and Upper Limb Tremor in a Patient with CMT Neuropathy.
Kumar, Rohini; Blackband, Jamie; Jain, Varun; Kugelmann, Lee; Subramony, Sub H; Wagle Shukla, Aparna.
Afiliação
  • Kumar R; Department of Neurology, Norman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, Florida, United States of America.
  • Blackband J; Department of Neurology, Norman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, Florida, United States of America.
  • Jain V; Department of Neurology, Norman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, Florida, United States of America.
  • Kugelmann L; Department of Neurology, Norman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, Florida, United States of America.
  • Subramony SH; Department of Neurology, Norman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, Florida, United States of America.
  • Wagle Shukla A; Department of Neurology, Norman Fixel Institute for Neurological Diseases, University of Florida, Gainesville, Florida, United States of America.
Article em En | MEDLINE | ID: mdl-38344215
ABSTRACT

Background:

Roussy-Lévy syndrome (RLS) is characterized by postural hand tremor seen in patients with familial autosomal dominant Charcot-Marie-Tooth (CMT) neuropathy. Phenomenology Shown This video demonstrates irregular, jerky bilateral kinetic, postural, rest tremor affecting the right > left hand, along with pes cavus and gait ataxia in a patient with CMT disease. Educational Value Pes cavus, tendon areflexia, sensory ataxia, and upper limb tremor should prompt consideration of CMT neuropathy. Highlights This video abstract depicts a bilateral hand tremor characteristic of Roussy-Lévy syndrome seen in patients with Charcot-Marie-Tooth disease neuropathy. The significance of the abstract lies in the phenomenology and the physiology of the tremor seen in patients with genetically confirmed duplication of PMP22 gene.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Pé Cavo Tipo de estudo: Etiology_studies / Qualitative_research Limite: Humans Idioma: En Revista: Tremor Other Hyperkinet Mov (N Y) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Pé Cavo Tipo de estudo: Etiology_studies / Qualitative_research Limite: Humans Idioma: En Revista: Tremor Other Hyperkinet Mov (N Y) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos