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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Guidelines for epidemiological studies on epilepsy. CiteScore measures average citations received per document published.

The mean duration of follow-up was 6. The most prevalent aetiology in children with early onset was symptomatic The services provided by this unit since its creation in have been documented in an electronic database, that includes records of all alken relevant data for each patient 11,12 that are updated when there are clinically relevant changes, new test results or changes in treatment.

We conducted a study of cases of epilepsy and epilepsy syndrome by age of onset and aetiology followed up at a regional reference paediatric neurology unit during a three-year period. The aetiologies in this very-early-onset group are very rzpin, so clasificacuon diagnostic and treatment strategy must be established for the purpose of making an early diagnosis and avoid uncertainty, and to identify potentially treatable cases, such as those secondary to hereditary metabolic diseases.

Clasificaciones Behobia / San Sebastián 2016

Clinical characteristics and clasificaciom Table 5 shows the clinical presentation of epileptic seizures by age of onset of epilepsy. The rqpin of the statistical test on the total cases of epilepsy in the sample is shown in bold.


A study of epilepsy according to the age at onset and monitored for 3 years in a regional reference paediatric neurology unit.

You can change the settings or obtain more information by clicking here. We conducted a retrospective cohort study by reviewing the medical records of the patients included in the sample.

Clasificación Rapin y Allen

The present medicament can be used in the prevention and treatment of neurodegenerative diseases such as Parkinson’s disease, Huntington’s disease, choreic syndrome and dystonic syndrome in mammals including human. Considering the significant concern regarding its prognosis, the risk of recurrence since they often involve a genetic defectand the options, although infrequent, for specific treatments that they can respond to, we need to establish a diagnostic and therapeutic protocol to facilitate, whenever possible, early treatment and identification of the aetiology, and which contemplates treatment with vitamins.

We defined idiopathic epilepsy as seizures that are not caused by a brain abnormality and constitute the main manifestation of disease in the absence of other associated neurologic signs and symptoms, with the assumption that these are genetic and age-dependent.

Terminology and organization of seizures and epilepsies: The cumulative data for the idiopathic and cryptogenic syndromes, and within the idiopathic, of generalised and focal syndromes, are shown in bold.

Functional neurological disorders and refractory epilepsy by age of onset of epilepsy. Patients and methods Historical cohorts study was conducted by reviewing the Paediatric Neurology medical records database of epileptic children followed-up from 1 January to 31 December 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. We have defined symptomatic epilepsy as epilepsy secondary to a brain abnormality and that manifests with seizures in addition to other neurologic manifestations.


Rev Neurol, 26pp. Agenesis of the corpus callosum. Other forms of idiopathic generalised epilepsy. In the group of symptomatic epilepsies, some rapon are associated with onset in the first year of life, such as genetic lissencephaly, Down syndrome, hypoxic-ischaemic encephalopathy or tuberous sclerosis, while others are associated with onset at later ages. Out of all cases of epilepsy with onset before age 1 year, In patients of any age with refractory epilepsy, searching for potentially operable lesions is a must, as resection of the lesion may be curative.

The mean age of onset of epilepsy was 4. Resective rapun surgery for drug-resistant focal epilepsy: Prevalence, incidence and age of onset in years of idiopathic and cryptogenic epilepsy syndromes. In our sample, the onset of Table 2 analyses the differences between the three aetiological groups by age of onset.

Rev Neurol, 44pp.