Traduction de «Childhood epilepsy » (Anglais → Français) :

Benign childhood epilepsy with centrotemporal EEG spikes Childhood epilepsy with occipital EEG paroxysms

Benign:myoclonic epilepsy in infancy | neonatal convulsions (familial) | Childhood absence epilepsy [pyknolepsy] Epilepsy with grand mal seizures on awakening Juvenile:absence epilepsy | myoclonic epilepsy [impulsive petit mal] | Nonspecific epileptic seizures:atonic | clonic | myoclonic | tonic | tonic-clonic

Jeavons syndrome is an idiopathic generalised form of reflex epilepsy characterised by childhood onset, unique seizure manifestations, striking light sensitivity, and possible occurrence of generalised tonic-clonic seizures. Onset occurs in childhood

childhood absence epilepsy | pyknolepsy

infantile spasm [ West syndrome | nodding spasm | salaam convulsion | salaam seizure | salaam attack | generalized flexion epilepsy syndrome | epilepsy syndrome | Blitz-Nick-Salaam-Krämpfe | eclampsia nutans | flexion spasm | infantile spastic epilepsy | infantile spastic epilepsy | jackknife spa ]

Rare childhood-onset epilepsy syndrome associated with infection and a biphasic clinical course. The initial symptom is a prolonged febrile seizure on day 1 (the first phase). Afterwards, patients have variable levels of consciousness from normal to

Childhood - juvenile - absence epilepsy

childhood behavioral disorders | childhood behavioural disorders

Definition: A type of pervasive developmental disorder that differs from childhood autism either in age of onset or in failing to fulfil all three sets of diagnostic criteria. This subcategory should be used when there is abnormal and impaired development that is present only after age three years, and a lack of sufficient demonstrable abnormalities in one or two of the three areas of psychopathology required for the diagnosis of autism (namely, reciprocal social interactions, communication, and restricted, stereotyped, repetitive behaviour) in spite of characteristic abnormalities in the other area(s). Atypical autism arises most often ...[+++]in profoundly retarded individuals and in individuals with a severe specific developmental disorder of receptive language. | Atypical childhood psychosis Mental retardation with autistic features

Whether the condition is diagnosed in childhood, such as with cerebral palsy, Tourette Syndrome, or epilepsy; in early adulthood, such as with multiple sclerosis; or later, as with Parkinson's or Alzheimer's disease, where most people are diagnosed after the age of 50; as the disease progresses, it takes a toll on a person's productivity.

Epilepsy can be present at any age, although its onset is most often in childhood or in later years of life.

Other children struggle with debilitating childhood diabetes, epilepsy and cerebral palsy.