Myotonic Steiner dystrophy in a family. Case Presentation

Myotonic dystrophy type I or Steinert's disease is of autosomal dominant genetic origin. It is characterized by multisystemic alterations such as musculoskeletal, cardiac, ocular, and endocrine and the most manifest that are usually neurological.The diagnosis is established by clinical data, el...

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Main Authors: María Octavina Rodríguez Roque (Author), Julio López Argüelles (Author), Ada Sánchez Lozano (Author), Didiesdle Herrera Alonso (Author), Leydi M. Sosa Águila (Author), Yansel Rodríguez Ramírez (Author)
Format: Book
Published: Centro Provincial de Información de Ciencias Médicas. Cienfuegos, 2020-02-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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