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1.
J Neurol Sci ; 427: 117506, 2021 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-34087568

RESUMEN

Epilepsy surgery is recommended in selected patients with Tuberous Sclerosis Complex (TSC). However, reports on predictive factors of seizure outcome are variable. Here we report on seizure and cognitive outcome of 35 TSC patients who received surgery for refractory epilepsy in 7 Italian centers over a period of 22 years (1997-2019). The rate of seizure-free individuals at last follow-up (mean 7.5 years, range 1-21 years) was 51%. Patients with longer follow-up (≥10 years) had a lower rate of Engel I outcome (11.1%) than those who received surgery in the last 10 years (65.4%, p = 0.003). Factors associated with Engel II, III, IV outcome in our cohort included: high number of cortical tubers (≥5); presence of subependymal nodules (SENs); seizure onset before age 1 year; and multifocal interictal epileptic discharges (IEDs) on electroencephalogram (EEG). A subset of patients evaluated with Vineland Adaptive Behaviour Scales (VABS) showed developmental gains, in line with their developmental trajectories, but no improvement in standard scores after surgery was noted. Our study demonstrates that the rates of successful seizure outcome of epilepsy surgery in TSC have improved in the last 10 years. More than half of the patients achieved seizure freedom, and a high proportion of affected individuals experienced a reduction in seizure burden and in antiseizure medications. A comprehensive assessment after surgery should be performed in TSC patients to evaluate the overall neurodevelopmental outcome, as measures that are based only on seizure control do not adequately identify the benefits of surgery on global functioning in these patients.


Asunto(s)
Epilepsia , Esclerosis Tuberosa , Electroencefalografía , Epilepsia/etiología , Epilepsia/cirugía , Humanos , Lactante , Estudios Retrospectivos , Convulsiones/epidemiología , Convulsiones/etiología , Convulsiones/cirugía , Resultado del Tratamiento , Esclerosis Tuberosa/complicaciones , Esclerosis Tuberosa/cirugía
2.
Brain Dev ; 32(1): 17-24, 2010 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19362436

RESUMEN

BACKGROUND: Rett syndrome is a severe neurodevelopmental disorder affecting almost exclusively females. Among Rett clinical variants, the early-onset seizure variant describes girls with early onset epilepsy and it is caused by mutations in CDKL5. METHODS: Four previously reported girls and five new cases with CDKL5 mutation, ranging from 14 months to 13 years, were evaluated by two clinical geneticists, classified using a severity score system based on the evaluation of 22 different clinical signs and compared with 128 classic Rett and 25 Zappella variant MECP2-mutated patients, evaluated by the same clinical geneticists. Clinical features were compared with previously described CDKL5 mutated patients. Both the statistical and the descriptive approach have been used to delineate clinical diagnostic criteria. RESULTS: All girls present epilepsy with onset varying from 10 days to 3 months. Patients may present different type of seizures both at onset and during the whole course of the disease; multiple seizure types may also occur in the same individual. After treatment with antiepileptic drugs patients may experience a short seizure-free period but epilepsy progressively relapses. Typical stereotypic hand movements severely affecting the ability to grasp are present. Psychomotor development is severely impaired. In the majority of cases head circumference is within the normal range both at birth and at the time of clinical examination. CONCLUSION: For the practical clinical approach we propose to use six necessary and eight supportive diagnostic criteria. Epilepsy with onset between the first week and 5 months of life, hand stereotypies, as well as severe hypotonia, are included among the necessary criteria.


Asunto(s)
Síndrome de Rett/diagnóstico , Convulsiones/diagnóstico , Adolescente , Edad de Inicio , Anticonvulsivantes/uso terapéutico , Niño , Preescolar , Epilepsia/diagnóstico , Epilepsia/tratamiento farmacológico , Epilepsia/genética , Femenino , Variación Genética , Cabeza/patología , Humanos , Lactante , Proteína 2 de Unión a Metil-CpG/genética , Hipotonía Muscular/diagnóstico , Hipotonía Muscular/genética , Mutación , Proteínas Serina-Treonina Quinasas/genética , Síndrome de Rett/tratamiento farmacológico , Síndrome de Rett/genética , Convulsiones/tratamiento farmacológico , Convulsiones/genética , Resultado del Tratamiento
3.
Brain Dev ; 29(2): 109-11, 2007 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-16876973

RESUMEN

We describe a case of hemiconvulsion-hemiplegia-epilepsy (HHE) syndrome documented by longitudinal magnetic resonance imaging (MRI). A two-year and nine-month-old boy had a prolonged hemiconvulsion during fever followed by right hemiparesis. Seven days later the imaging abnormality on T2 and diffusion-weighted images (DWI) was limited to the white matter of the left hemisphere. One month later severe gliosis and unilateral brain atrophy were already evident. MRI is useful in the early stages of prolonged seizures and T2 and DWI abnormalities appear to be well correlated with parenchymal damage that results from sustained ictal activity. The neuroradiological findings in our case and in the few HHE patients reported in the literature seem to be very characteristic and, if confirmed in larger series, could permit an early diagnosis.


Asunto(s)
Imagen de Difusión por Resonancia Magnética , Epilepsia , Hemiplejía , Angiografía por Resonancia Magnética , Preescolar , Epilepsia/complicaciones , Epilepsia/diagnóstico por imagen , Epilepsia/patología , Estudios de Seguimiento , Lateralidad Funcional , Hemiplejía/complicaciones , Hemiplejía/diagnóstico por imagen , Hemiplejía/patología , Humanos , Masculino , Cintigrafía
4.
Neurol Sci ; 25(5): 264-73, 2004 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15624084

RESUMEN

The objective was to evaluate the quality of life of young Italian patients with epilepsy and to investigate the influence of epilepsy medical variables on patients' quality of life. The settings were the Department of Paediatrics, University of Padua; Children's Hospital Giovanni XXIII, Bari; and three schools of South Italy. A sample of 285 subjects was selected: 140 subjects affected by idiopathic and cryptogenic epilepsy (classified according to the International League Against Epilepsy criteria) and 145 control subjects. Data derived from the comparison between the two groups throughout "Epilepsy and children questionnaire" confirmed the negative epilepsy impact on the young patients' quality of life: in fact they scored significantly lower on psychological and social domains (p

Asunto(s)
Epilepsia/psicología , Calidad de Vida/psicología , Adolescente , Afecto/fisiología , Factores de Edad , Edad de Inicio , Niño , Epilepsia/epidemiología , Femenino , Humanos , Italia/epidemiología , Masculino , Reproducibilidad de los Resultados , Instituciones Académicas , Convulsiones/fisiopatología , Factores Sexuales , Conducta Social , Factores Socioeconómicos , Encuestas y Cuestionarios
5.
Epilepsia ; 40(12): 1799-803, 1999 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-10612347

RESUMEN

PURPOSE: A locus for benign familial convulsions (BFICs) has been recently mapped on chromosome 19q12-13.1 by studying five families of Italian descent. The main goal of this study was to investigate the role of this locus in a set of seven newly identified families with at least three affected cases. METHODS: Five polymorphic microsatellite markers covering the BFIC locus on chromosome 19q have been typed, and parametric linkage analysis has been performed to analyze the segregation of the BFIC locus within our families. RESULTS: Cumulative 2-point lod scores and multipoint analysis showed no evidence of linkage between chromosome 19 markers and the BFIC phenotype. The analysis of family-specific 2-point lod scores and haplotypes, however, indicated the presence of linkage to chromosome 19q in a single family, suggesting genetic heterogeneity within our family sample. CONCLUSIONS: Our study demonstrates that the previously reported BFIC locus on chromosome 19q12-13.1 is not a major locus for BFICs. We suggest that genetic heterogeneity may have generated our discordant linkage findings, as it was reported in benign familial neonatal convulsions, a related idiopathic mendelian syndrome.


Asunto(s)
Cromosomas Humanos Par 19/genética , Familia , Convulsiones/genética , Mapeo Cromosómico , Femenino , Ligamiento Genético , Marcadores Genéticos , Genotipo , Humanos , Italia/epidemiología , Masculino , Convulsiones/epidemiología
6.
Brain Dev ; 17(1): 64-8, 1995.
Artículo en Inglés | MEDLINE | ID: mdl-7762767

RESUMEN

The authors describe 7 new cases of Angelman syndrome (AS: 3 males and 4 females) diagnosed on the basis of clinical features (dysmorphic facial features, severe mental retardation with absent speech, peculiar jerky movements, ataxic gait and paroxysms of inappropriate laughter) and neurophysiological findings. Failure to detect deletion of the long arm of chromosome 15 or the absence of epileptic seizure were not considered sufficient to exclude a diagnosis of AS. Feeding problems, developmental delay and early signs of ataxia, especially tremor on handling objects and unstable posture when seated, proved effective as clinical markers for early diagnosis of AS. The EEG patterns characteristic of AS were found within the first 2 years of life (under 18 months in the majority of cases). The authors conclude that AS should be included in differential diagnosis in a child aged under 12 months having cryptogenic psychomotor retardation with prevalent language compromise. Repeat EEG recordings are needed to check for the typical trace, and cytogenetic investigations are mandatory.


Asunto(s)
Síndrome de Angelman/diagnóstico , Electroencefalografía , Niño , Preescolar , Femenino , Humanos , Lactante , Masculino , Neurofisiología
7.
Brain Dev ; 16(3): 257-9, 1994.
Artículo en Inglés | MEDLINE | ID: mdl-7943616

RESUMEN

A 2-day old girl with status epilepticus, unresponsive to maximum pharmacological intervention, is reported. Findings of brain and cardiac lesions pointed to the diagnosis of tuberous sclerosis. One of the brain lesions was unusually large, occupying most of the right temporo-parietal lobe.


Asunto(s)
Encefalopatías/congénito , Convulsiones/congénito , Anticonvulsivantes/uso terapéutico , Encefalopatías/complicaciones , Encefalopatías/patología , Electroencefalografía , Femenino , Neoplasias Cardíacas/complicaciones , Neoplasias Cardíacas/patología , Humanos , Recién Nacido , Imagen por Resonancia Magnética , Rabdomiosarcoma/complicaciones , Rabdomiosarcoma/patología , Esclerosis , Convulsiones/complicaciones , Convulsiones/patología , Estado Epiléptico/complicaciones , Estado Epiléptico/patología , Tomografía Computarizada por Rayos X
8.
Brain Dev ; 13(4): 238-41, 1991 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-1957972

RESUMEN

Neurophysiological studies have shown defects in peripheral conduction in up to 75% of adults with end-stage renal disease (ESRD), though abnormalities of central conduction seem more variable. There are no comparable pediatric data. We therefore measured median nerve somatosensory evoked potentials (SEPs) in 10 children with ESRD, maintained by hemodialysis, who had no neurological signs or symptoms, and compared the results with those for age-matched controls. The latencies of N9, P14, N20 and P22, and interpeak latencies, N9-N20, N9-P14 and P14-N20, were not significantly different between the two groups (Student's t test). However, the children with ESRD were significantly retarded in growth and when arm length was taken into account, a significant difference in peripheral conduction was revealed. There was no correlation with other indexes of disease severity (parathormone, aluminium, Hb, Na, K, Cl, BUN and creatinine). SEPs appear to reflect subclinical changes in peripheral conduction in sensory pathways in children with ESRD which are not correlated with other measures of disease severity.


Asunto(s)
Potenciales Evocados Somatosensoriales/fisiología , Uremia/fisiopatología , Adolescente , Niño , Preescolar , Electroencefalografía , Femenino , Humanos , Lactante , Masculino , Conducción Nerviosa/fisiología , Tiempo de Reacción , Análisis de Regresión
12.
Headache ; 30(10): 646-9, 1990 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-2272814

RESUMEN

99mTC HM-PAO SPECT brain imaging was performed during the headache-free period in 19 young migraineurs, affected by common migraine (CM, 10 cases), classic migraine (CLM, 6 cases) and hemiplegic migraine (HM, 3 cases). SPECT findings were negative in all 10 patients with CM, in 3 cases of CLM and in 2 cases of HM. Positive findings in the remaining 4 patients (3 cases of CLM and 1 of HM) showed a decreased tracer distribution in the temporo-occipital regions (2 cases) and parietal regions (2 cases): the two with decreased temporo-occipital perfusion reported prodromal symptoms exclusively contralateral to the areas of hypoperfusion. An impaired regional cerebral vascular autoregulation may exist even during headache-free intervals in patients suffering from classic and hemiplegic migraine.


Asunto(s)
Circulación Cerebrovascular , Trastornos Migrañosos/diagnóstico por imagen , Tomografía Computarizada de Emisión de Fotón Único , Adolescente , Niño , Femenino , Humanos , Masculino , Trastornos Migrañosos/fisiopatología
13.
Pediatr Med Chir ; 11(1): 89-91, 1989.
Artículo en Italiano | MEDLINE | ID: mdl-2717492

RESUMEN

A case of late onset focal epilepsy in a mentally and neurologically normal girl in which the MRI showed a focal heterotopia is presented. The efficacy of this new procedure in detecting migratory disorders is discussed and the scanty literature reviewed. This case suggests that in the future more cases of epilepsy previously classified as "cryptogenetic" will be demonstrated as secondary to developmental abnormalities.


Asunto(s)
Neoplasias Encefálicas/diagnóstico , Encéfalo , Coristoma/diagnóstico , Epilepsia/etiología , Imagen por Resonancia Magnética , Neoplasias Encefálicas/complicaciones , Corteza Cerebral , Niño , Coristoma/complicaciones , Electroencefalografía , Femenino , Humanos , Tomografía Computarizada por Rayos X
14.
Pediatr Med Chir ; 10(6): 595-601, 1988.
Artículo en Italiano | MEDLINE | ID: mdl-3244539

RESUMEN

Clinical and EEG findings have been analysed in six patients with Rett syndrome with a mean follow-up of 3 years and 9 months. After reviewing the diagnostic criteria for inclusion, which are essentially clinical, we emphasize two aspects which have been shortly considered in the literature: a) epileptic seizures, b) peculiar differential characteristics between primary autism and the Rett syndrome behaviour. Moreover, we underline the importance of serial EEG poligraphic records for early diagnosis.


Asunto(s)
Trastorno Autístico/diagnóstico , Electroencefalografía , Epilepsia/diagnóstico , Discapacidad Intelectual/diagnóstico , Trastornos del Movimiento/diagnóstico , Preescolar , Femenino , Estudios de Seguimiento , Humanos , Lactante , Síndrome
15.
Pediatr Med Chir ; 4(4): 443-6, 1982.
Artículo en Italiano | MEDLINE | ID: mdl-7170219

RESUMEN

After having illustrated the varied pathology of the umbilical region, the A.A. describe a case of a suppurated cyst of the urachus (pyourachus) in a 12 years old girl. They underline the many types of onset as well as of evolution of the urachal cysts and the differential diagnosis of them. Fistolography, when possible, is the decisive examination. Obviously the treatment may be only surgical. The premonitory signs for a precocious diagnosis are indicated.


Asunto(s)
Quiste del Uraco/diagnóstico , Niño , Diagnóstico Diferencial , Femenino , Hemorragia/etiología , Humanos , Menorragia/diagnóstico , Quiste del Uraco/complicaciones , Quiste del Uraco/cirugía
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