The main identifiable risk factor in the clinical history is the presence of an older sibling with ASD, such that 1 in 5 children with older siblings with ASD will have an ASD diagnosis by age 3, being more frequent among males. Parental age is also a risk factor …
Category archives: Neurological diseases
Cytomegalovirus congenital.
Indications for CMV PCR in urine within the first 2 weeks of life for the diagnosis of congenital CMV.
Diagnosis comorbid ASD-DI and genetic diagnosis.
Disfemia-stuttering.
Website of the Spanish Stuttering Foundation with specific resources for the pediatric age group.
Springer video atlas of movement disorders.
Click on the icon in the right corner to access one of the 97 posted videos.
Tik Tok tics.
Dystonia myoclonus, not all tics.
Genetics of movement disorders.
The MDSGene website contains a directory of currently well-established movement disorders of genetic origin.
Neurocutaneous syndromes.
Aplasia cutis congenita. Nevus sebaceous of Jadassohn. Epidermal nevus. Schimmelpenning-Feuerstein-Mims syndrome. Pringle-Bourneville syndrome (tuberous sclerosis). Neurofibromatosis type 1 (von Recklinghausen). Incontinentia pigmenti. Congenital melanocytic nevus. Neurocutaneous melanosis. Xeroderma pigmentosum. Cockayne syndrome. Ehlers-Danlos syndrome. Klippel-Trenaunay-Weber syndrome. Proteus syndrome. Sjögren-Larsson syndrome. Sturge-Weber syndrome. Blue rubber bleb nevus syndrome. Incontinentia pigmenti …
