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Musculoskeletal Diseases > Muscular Diseases > Paralyses, Familial Periodic > Hypokalemic Periodic Paralysis
Nervous System Diseases > Neuromuscular Diseases > Muscular Diseases > Paralyses, Familial Periodic > Hypokalemic Periodic Paralysis
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Metal Metabolism, Inborn Errors > Paralyses, Familial Periodic > Hypokalemic Periodic Paralysis
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Metal Metabolism, Inborn Errors > Paralyses, Familial Periodic > Hypokalemic Periodic Paralysis

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Hypokalemic Periodic Paralysis  

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Tipo

  • mesh:Descriptor

Definición

  • An autosomal dominant familial disorder characterized by recurrent episodes of skeletal muscle weakness associated with falls in serum potassium levels. The condition usually presents in the first or second decade of life with attacks of trunk and leg paresis during sleep or shortly after awakening. Symptoms may persist for hours to days and generally are precipitated by exercise or a meal high in carbohydrates. (Adams et al., Principles of Neurology, 6th ed, p1483)

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Familial Hypokalemic Periodic Paralysis
  • HOKPP
  • Hypokalemic Periodic Paralysis, Familial
  • HYPOKPP
  • HYPOPP
  • Paralysis, Hypokalemic Periodic
  • Periodic Paralysis- Hypokalemic
  • Primary Hypokalemic Periodic Paralysis
  • Westphall Disease

En otras lenguas

  • Paralysie périodique hypokaliémique

    francés

  • Maladie de Westphal
  • Maladie de Westphall
  • Paralysie périodique hypokaliémique de Westphal
  • Paralysie périodique primitive hypokaliémique de Westphal

URI

http://data.loterre.fr/ark:/67375/JVR-F3JPD786-W

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