Category archives: Neurological diseases
Cromatinopatías.
Sinaptopatías.
The comorbid diagnosis of ASD and ID requires that social communication be below what is expected for the general developmental level (Criterion E of DSM-5). The clinical differentiation between both entities in young children or those with severe disability is particularly complex, requiring a multidisciplinary approach and systematic phenotypic refinement.
SLC, solute carriers
The prevalence of ASD in individuals with ID is higher than in the general population, and its precise identification is fundamental for designing a specific therapeutic plan.
CSWS
Continuous spike-wave during sleep is an age-dependent epileptic encephalopathy characterized by the presence of status epilepticus during deep sleep, and significant cognitive-behavioral consequences. It is also known as Penelope syndrome. Landau-Kleffner syndrome (or epilepsy-aphasia spectrum) is a subtype of this disease, in which the neurological deficit is …
Newborn Screening in other countries
Parental age and neurodevelopment.
Neuroplacentology.
Placental disease has consequences on the fetal brain and the newborn, and it is necessary to understand some of the placental pathologies that may be responsible for future neurological problems.
