peer reviewedSummary : Down syndrome is one of best caracterized genetic syndromes. Its phenotype includes specific morphological features, mental retardation and several organic impairments such as cardiac malformations, cutaneous disorders and immunologic abnormalities. Beside these disturbances neurological disorders have been less considered or thought to be the expression of the mental retardation. However it is important to pay attention to the high incidence of epilepsy such as West syndrome in infants and “Late-Onset of myoclonic epilepsy in Down Syndrome” in the adult. They might required specific treatment. ADHD as well as autistic behavior may be difficult to diagnose especially in children with severe mental retardation. The...
Wolfram syndrome type 1 (WS1) is a rare autosomal recessive neurodegenerative disorder characterized...
En dépit des progrès de la médecine, la prise en charge des patients récupérant d'un coma constitue ...
L’adrénoleucodystrophie (ALD) liée à l’X est une maladie génétique liée au chromosome sexuel X. Les ...
Epilepsy is a common chronic disease affecting preferentially patients with intellectual disabilitie...
Early-onset schizophrenia (EOS) is a rare, severe and neurodevelopmental form of schizophrenia begin...
Early-onset schizophrenia (EOS) is a rare, severe and neurodevelopmental form of schizophrenia begin...
Early-onset schizophrenia (EOS) is a rare, severe and neurodevelopmental form of schizophrenia begin...
Epilepsy is defined as the repetition of seizures, with varied symptomatology, whose spontaneous and...
editorial reviewedLe chapitre propose une analyse des données disponibles en ce qui concerne 4 syndr...
Epilepsy is defined as the repetition of seizures, with varied symptomatology, whose spontaneous and...
Le syndrome de Down (DS) est la cause génétique la plus fréquente de déficience intellectuelle (ID) ...
peer reviewedPreferential cerebellar localization during a severe methadone intoxication is explaine...
Developmental disorders (DD) include malformative disorders and neurodevelopmental disorders such as...
Developmental disorders (DD) include malformative disorders and neurodevelopmental disorders such as...
La maladie de Lafora est une forme rare et grave d’épilepsie myoclonique progressive (EMP). Elle est...
Wolfram syndrome type 1 (WS1) is a rare autosomal recessive neurodegenerative disorder characterized...
En dépit des progrès de la médecine, la prise en charge des patients récupérant d'un coma constitue ...
L’adrénoleucodystrophie (ALD) liée à l’X est une maladie génétique liée au chromosome sexuel X. Les ...
Epilepsy is a common chronic disease affecting preferentially patients with intellectual disabilitie...
Early-onset schizophrenia (EOS) is a rare, severe and neurodevelopmental form of schizophrenia begin...
Early-onset schizophrenia (EOS) is a rare, severe and neurodevelopmental form of schizophrenia begin...
Early-onset schizophrenia (EOS) is a rare, severe and neurodevelopmental form of schizophrenia begin...
Epilepsy is defined as the repetition of seizures, with varied symptomatology, whose spontaneous and...
editorial reviewedLe chapitre propose une analyse des données disponibles en ce qui concerne 4 syndr...
Epilepsy is defined as the repetition of seizures, with varied symptomatology, whose spontaneous and...
Le syndrome de Down (DS) est la cause génétique la plus fréquente de déficience intellectuelle (ID) ...
peer reviewedPreferential cerebellar localization during a severe methadone intoxication is explaine...
Developmental disorders (DD) include malformative disorders and neurodevelopmental disorders such as...
Developmental disorders (DD) include malformative disorders and neurodevelopmental disorders such as...
La maladie de Lafora est une forme rare et grave d’épilepsie myoclonique progressive (EMP). Elle est...
Wolfram syndrome type 1 (WS1) is a rare autosomal recessive neurodegenerative disorder characterized...
En dépit des progrès de la médecine, la prise en charge des patients récupérant d'un coma constitue ...
L’adrénoleucodystrophie (ALD) liée à l’X est une maladie génétique liée au chromosome sexuel X. Les ...