Talk:Channelopathy

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Archived wikipedia table[edit source | reply | new]

Types[edit source | reply | new]

Condition Channel type
Alternating hemiplegia of childhood Na⁺/K⁺-ATPase
Bartter syndrome various by type
Brugada syndrome various, by type
Catecholaminergic polymorphic ventricular tachycardia (CPVT) Calcium channel
Congenital hyperinsulinism Inward-rectifier potassium ion channel
Cystic fibrosis Chloride channel
Dravet Syndrome Voltage-gated sodium channel
Episodic Ataxia Voltage-gated potassium channel
Erythromelalgia Voltage-gated sodium channel
Generalized epilepsy with febrile seizures plus Voltage-gated sodium channel
Familial hemiplegic migraine various
Associated with one particular disabling form of Fibromyalgia[1] Voltage-gated sodium channel
Hyperkalemic periodic paralysis Voltage-gated sodium channel
Hypokalemic periodic paralysis Voltage-gated sodium channel

or
voltage-dependent calcium channel (calciumopathy)

Lambert-Eaton myasthenic syndrome Voltage-gated calcium channel
Long QT syndrome

main type Romano-Ward syndrome

various, by type
Malignant hyperthermia Ligand-gated calcium channel
Mucolipidosis type IV Non-selective cation channel
Myotonia congenita Voltage-dependent chloride channel
Neuromyelitis optica Aquaporin-4 water channel
Neuromyotonia Voltage-gated potassium channel
Nonsyndromic deafness various
Paramyotonia congenita
(a periodic paralysis)
 Voltage-gated sodium channel
Retinitis pigmentosa
(some forms)
 Ligand-gated non-specific ion channels
Short QT syndrome various potassium channels suspected
Timothy syndrome Voltage-dependent calcium channel
Tinnitus Voltage-gated potassium channel of the KCNQ family
Seizure Voltage-dependent potassium channel[2][3]

Voltage-dependent potassium channel [4][5]

Source: Wikipedia

Discussion[edit source | reply | new]

  1. ↑ Vargas-Alarcon G, Alvarez-Leon E, Fragoso JM, Vargas A, Martinez A, Vallejo M, Martinez-Lavin M (2012). "A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia". J Rheumatol Suppl. 19: 13:23. doi:10.1186/1471-2474-13-23. PMC 3310736. PMID 22348792. Cite has empty unknown parameter: |1= (help)
  2. ↑ Hunter, JV; Moss, AJ (January 2009). "Seizures and arrhythmias: Differing phenotypes of a common channelopathy?". Neurology (journal). 72 (3): 208–9. doi:10.1212/01.wnl.0000339490.98283.c5. PMID 19153369. Retrieved April 30, 2009. via= Missing pipe in: |quote= (help)
  3. ↑ Mulley, SF; Scheffer, IE; Petrou; Berkovic (April 2003). "Channelopathies as a genetic cause of epilepsy". Current Opinion in Neurology. 16 (2): 171–6. doi:10.1097/00019052-200304000-00009. PMID 12644745. Retrieved April 30, 2009.
  4. ↑ Hunter, JV; Moss, AJ (January 2009). "Seizures and arrhythmias: Differing phenotypes of a common channelopathy?". Neurology (journal). 72 (3): 208–9. doi:10.1212/01.wnl.0000339490.98283.c5. PMID 19153369. Retrieved April 30, 2009.
  5. ↑ Mulley, SF; Scheffer, IE; Petrou; Berkovic (April 2003). "Channelopathies as a genetic cause of epilepsy". Current Opinion in Neurology. 16 (2): 171–6. doi:10.1097/00019052-200304000-00009. PMID 12644745. Retrieved April 30, 2009.
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