Title of article :
Neurological disorders caused by inherited ion-channel mutations
Author/Authors :
Dimitri M Kullmann، نويسنده , , Michael G Hanna، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2002
Pages :
10
From page :
157
To page :
166
Abstract :
Summary Several neurological diseases-including neuromuscular disorders, movement disorders, migraine, and epilepsy-are caused by inherited mutations of ion channels. The list of these “channelopathies” is expanding rapidly, as is the phenotypic range associated with each channel. At present the best understood channelopathies are those that affect muscle-fibre excitability. These channelopathies produce a range of disorders which include: periodic paralysis, myotonias, malignant hyperthermia, and congenital myasthenic syndromes. By contrast, the mechanisms of diseases caused by mutations of ion channels that are expressed in neurons are less well understood. However, as for the muscle channelopathies, a striking feature is that many neuronal channelopathies cause paroxysmal symptoms. This review summarises the clinical features of the known neurological channelopathies, within the context of the functions of the individual ion channels.
Journal title :
Lancet Neurology
Serial Year :
2002
Journal title :
Lancet Neurology
Record number :
800481
Link To Document :
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