Clasificación TEL de Rapin y Allen. Uploaded by. Javiera Fernanda Eyzaguirre García · fisioterapia_orofacial_y_de_reeducacion_de_la_deglucion. Non‐specialists can identify three types of developmental language disorder. (1) mixed receptive/expressive disorders, which impair phonology, syntax, and. Desde la clasificación de Rapin y Allen () han surgido algunas nuevas, como la de Crespo-Eguílaz y Narbona (), que diferen- cian tres subgrupos a .

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Clasificaciones Behobia / San Sebastián 2016

Adhering to the definition of the International League Against Epilepsy ILAE14 we defined refractory epilepsy as failure of adequate trials of two tolerated and appropriately chosen and used antiepileptic drug schedules whether as monotherapies or in combination to achieve sustained seizure freedom.

The younger the age of onset, the greater the percentage of refractory disease and of neurologic disorders: Epileptic Disord, 15pp. The cumulative data for the idiopathic and cryptogenic syndromes, and within the idiopathic, of generalised and focal syndromes, are shown allem bold. The age of onset is a decisive factor in the approach to childhood epilepsy; in older children, neuroimaging tests and electroencephalography may be sufficient, but infants may require extensive workups metabolic and genetic.

Clasificación Rapin y Allen

Rev Neurol, 44pp. Benign partial epilepsy of childhood with occipital paroxysms. Well-defined syndromes usually appear during this period, for instance, epilepsy with absence seizures and benign childhood epilepsy with centrotemporal spikes, 7 which were the most prevalent epileptic syndromes in this age group in our study.


Epilepsy presented as infantile spasms in Table 2 analyses the differences between the three aetiological groups by age of onset. J Child Neurol, 9pp.

The population under study consisted of all patients aged more than 1 month with a diagnosis of epilepsy assessed for the first time or in follow-up visits at the Unit of Paediatric Neurology of the Hospital Miguel Servet of Zaragoza over a three-year period from January 1, to December 31, Seizure, 21raapin. Fecha de la solicitud, orden descendente.

Of the two cases of genetic lissencephaly, one was due to a mutation in the LIS1 gene and the other to a mutation in the EN2 gene.

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In the three years under study, new cases of epilepsy were diagnosed, while the rest of assessments corresponded to patients in follow-up. For purposes of screening agents for treatment of neurodegenerative disease, oxidative stress in the neuronal cells is stimulated by introducing a mixture of metal-ions clasificzcion hydrogen peroxide.

The absolute frequencies and percentages over the total sample of epilepsies in each age group are shown in bold. Rev Neurol, 54 dlasificacion, pp. Epilepsy with myoclonic-astatic seizures. Epilepsia, 30pp. Rev Neurol, 32pp.

Rev Neurol, 28pp. Absence epilepsy and benign childhood epilepsy with centro-temporal spikes are the idiopathic epileptic syndromes most prevalent, and the most prevalent symptomatic epilepsies are prenatal encephalopathies. Comparison of age of onset of epilepsy by type of seizure Kruskal—Wallis test with Bonferroni correction.


Table 4 summarises the incidence, prevalence and age of onset of symptomatic epilepsies by aetiology. In our study, In our sample, the onset of Another key factor is the age at the first seizure which depends on the aetiologywith early ages generally associated with poorer outcomes.

Clasificaciones Behobia / San Sebastián

We assessed prognosis taking into account treatment effectiveness refractory disease and the impact on neurologic function. An Pediatr Barc67pp. The diagnosis of rrapin was established in Epilepsy was categorised as symptomatic in patients In cases with early onset, epilepsy is due much more frequently to a severe brain abnormality, responding poorly to treatment and carrying a poor neurologic and neurodevelopmental prognosis.

Rapon idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures. Historical cohorts study was conducted by reviewing the Paediatric Neurology medical records database of epileptic children followed-up from 1 January to 31 December