|
Differential Diagnosis of Channelopathies |
| Thyrotoxic hypokalemic periodic paralysis (TPP) |
| Primary (or familial) hypokalemic periodic paralysis (hypoPP) |
| Hyperkalemic periodic paralysis (hyperPP) |
| Paramyotonia congenita (PMC) |
| Potassium-aggravated myotonia (PAM) [22, 23] (includes myotonia fluctuans [24], acetazolamide-responsive myotonia [25], and myotonia permanens [26]) |
| Myotonia congenita, both recessive and dominant (MC) |
| Andersen-Tawil syndrome (ATS) (formerly Andersen syndrome) |
| Hyperaldosteronism and physiologically similar states |
| Renal tubular acidosis Type IV (RTA) |
| Diuretic abuse |
| Myasthenia gravis |
Levitt Journal of Translational Medicine 2008 6:18 doi:10.1186/1479-5876-6-18 |