Medical Definition of Familial periodic paralysis

1. A rare inherited disorder, affecting men more often than women, characterised by intermittent episodes of muscle weakness or paralysis. One form, known as hypokalaemic periodic paralysis, is an autosomal recessive disorder that is characterised by bouts of muscle weakness (or paralysis) accompanied by low serum potassium levels. Inheritance: autosomal recessive. Incidence: 1 in 100,000. (27 Sep 1997)

Lexicographical Neighbors of Familial Periodic Paralysis

familial intestinal polyposis
familial juvenile nephrophthisis
familial lipodystrophy
familial lipoprotein lipase deficiency
familial lipoprotein lipase inhibitor
familial mediterranean fever
familial mental retardation 1
familial mental retardation protein
familial microcytic anaemia
familial multiple endocrine adenomatosis
familial nephrosis
familial neuroviscerolipidosis
familial nonhaemolytic nonobstructive jaundice
familial nonhemolytic jaundice
familial paroxysmal rhabdomyolysis
familial periodic paralysis (current term)
familial polyposis
familial polyposis coli
familial pseudoinflammatory macular degeneration
familial pseudoinflammatory maculopathy
familial pyridoxine-responsive anaemia
familial recurrent polyserositis
familial screening
familial spinal muscular atrophy
familial tremor
familial white folded dysplasia
familiality
familially
familiar

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