Mutations of theSCN1Agene in acute encephalopathy

    loading  Checking for direct PDF access through Ovid

Abstract

Purpose:

Acute encephalopathy is the most serious complication of pediatric viral infections, such as influenza and exanthema subitum. It occurs worldwide, but is most prevalent in East Asia. Recently, there have been sporadic case reports of epilepsy/febrile seizure and acute encephalopathy with a neuronal sodium channel alpha 1 subunit (SCN1A) mutation. To determine whetherSCN1Amutations are a predisposing factor of acute encephalopathy, we sought to identifySCN1Amutations in a large case series of acute encephalopathy including various syndromes.

Methods:

We analyzed theSCN1Agene in 87 patients with acute encephalopathy, consisting of 20 with acute necrotizing encephalopathy (ANE), 61 with acute encephalopathy with biphasic seizures and late reduced diffusion (AESD), and six with nonspecific (unclassified) acute encephalopathy.

Key Findings:

Three patients had distinct point mutations. Two of them had epileptic seizures prior to acute encephalopathy. Clinical and neuroradiologic findings of acute encephalopathy were diverse among the three patients, although all had a prolonged and generalized seizure at its onset. The first patient with V982L had partial epilepsy and AESD. The second patient with M1977L had febrile seizures and nonspecific acute encephalopathy. The third patient with R1575C had no seizures until the onset of ANE. M1977L was a novel mutation, whereas the remaining two, V982L and R1575C, have previously been reported in cases of Dravet syndrome and acute encephalopathy, respectively.

Significance:

These findings provide further evidence thatSCN1Amutations are a predisposing factor for the onset of various types of acute encephalopathy.

Related Topics

    loading  Loading Related Articles