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Results 1 - 10 of 18 for Channelopathy
  1. Channelopathy-associated congenital insensitivity to pain 
    Channelopathy-associated congenital insensitivity to pain is a condition that inhibits the ability to perceive physical pain. ... have shorter life expectancies.The first signs of channelopathy-associated congenital insensitivity to pain often occur when ...
    https://medlineplus.gov/...sociated-congenital-insensitivity-to-pain - Genetics
  2. Andersen-Tawil syndrome 
    ... The long QT syndrome family of cardiac ion channelopathies: a HuGE review. Genet Med. 2006 Mar;8( ... Tristani-Firouzi M, Etheridge SP. Kir 2.1 channelopathies: the Andersen-Tawil syndrome. Pflugers Arch. 2010 Jul; ...
    https://medlineplus.gov/genetics/condition/andersen-tawil-syndrome - Genetics
  3. Episodic ataxia 
    ... MG. Episodic ataxia type 1: a neuronal potassium channelopathy. Neurotherapeutics. 2007 Apr;4(2):258-66. doi: ...
    https://medlineplus.gov/genetics/condition/episodic-ataxia - Genetics
  4. Short QT syndrome 
    Short QT syndrome is a condition that can cause a disruption of the heart's normal rhythm (arrhythmia). In people with this condition, the heart (cardiac) muscle ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
  5. Familial atrial fibrillation 
    Familial atrial fibrillation is an inherited abnormality of the heart's normal rhythm. Atrial fibrillation is characterized by episodes of uncoordinated electrical ...
    https://medlineplus.gov/.../condition/familial-atrial-fibrillation - Genetics
  6. Hereditary hyperekplexia 
    Hereditary hyperekplexia is a condition in which affected infants have increased muscle tone (hypertonia) and an exaggerated startle reaction to unexpected stimuli, ...
    https://medlineplus.gov/genetics/condition/hereditary-hyperekplexia - Genetics
  7. Clouston syndrome 
    Clouston syndrome is a form of ectodermal dysplasia, a group of about 150 conditions characterized by abnormal development of some or all of the ectodermal structures, ...
    https://medlineplus.gov/genetics/condition/clouston-syndrome - Genetics
  8. Hypokalemic periodic paralysis 
    ... 02)00007-x. Citation on PubMed Cannon SC. Channelopathies of skeletal muscle excitability. Compr Physiol. 2015 Apr; ... Jurkat-Rott K, Rudel R. Periodic paralysis: understanding channelopathies. Curr Neurol Neurosci Rep. 2002 Jan;2(1): ...
    https://medlineplus.gov/.../condition/hypokalemic-periodic-paralysis - Genetics
  9. Hyperkalemic periodic paralysis 
    ... Holzherr B, Fauler M, Lehmann-Horn F. Sodium channelopathies of skeletal muscle result from gain or loss ...
    https://medlineplus.gov/.../hyperkalemic-periodic-paralysis - Genetics
  10. Paramyotonia congenita 
    ... PubMed Tamaoka A. Paramyotonia congenita and skeletal sodium channelopathy. Intern Med. 2003 Sep;42(9):769-70. ...
    https://medlineplus.gov/genetics/condition/paramyotonia-congenita - Genetics
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