ey Findings: Mean age at the time of the study was 13.5 +/- 11 years. Mean age at seizure onset was 15.5 +/- 11 months (range 9-38). All patients experienced clusters of either focal or generalized seizures, precipitated during febrile illness in five patients. Attacks were very frequent at onset, but they became less numerous during follow-up. Ictal electroencephalography (EEG) showed temporal lobe involvement in five patients. Periictal EEG showed focal or multifocal epileptiform and slow abnormalities. Cognitive impairment became obvious after seizure onset in three patients and was associated with autistic features in two. Genetic analysis revealed five new and one known de novo PCDH19 mutation that were missense in four and frameshift in two. Variants are clustered in the large exon 1, corresponding to the extracellular domain of the PCDH19 protein.

Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations / Specchio N; Marini C; Terracciano A; Mei D; Trivisano M; Sicca F; Fusco L; Cusmai R; Darra F; Bernardina BD; Bertini E; Guerrini R; Vigevano F. - In: EPILEPSIA. - ISSN 0013-9580. - STAMPA. - 52(7):(2011), pp. 1251-1257. [10.1111/j.1528-1167.2011.03063.x]

Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations

Marini C;GUERRINI, RENZO;
2011

Abstract

ey Findings: Mean age at the time of the study was 13.5 +/- 11 years. Mean age at seizure onset was 15.5 +/- 11 months (range 9-38). All patients experienced clusters of either focal or generalized seizures, precipitated during febrile illness in five patients. Attacks were very frequent at onset, but they became less numerous during follow-up. Ictal electroencephalography (EEG) showed temporal lobe involvement in five patients. Periictal EEG showed focal or multifocal epileptiform and slow abnormalities. Cognitive impairment became obvious after seizure onset in three patients and was associated with autistic features in two. Genetic analysis revealed five new and one known de novo PCDH19 mutation that were missense in four and frameshift in two. Variants are clustered in the large exon 1, corresponding to the extracellular domain of the PCDH19 protein.
2011
52(7)
1251
1257
Specchio N; Marini C; Terracciano A; Mei D; Trivisano M; Sicca F; Fusco L; Cusmai R; Darra F; Bernardina BD; Bertini E; Guerrini R; Vigevano F
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/606354
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