Ad
related to: landau kleffner syndrome children
Search results
Results From The WOW.Com Content Network
Landau–Kleffner syndrome (LKS), also called infantile acquired aphasia, acquired epileptic aphasia, [1] or aphasia with convulsive disorder, is a rare neurological syndrome that develops during childhood. [2] It is named after William Landau and Frank Kleffner, who characterized it in 1957 with a diagnosis of six children. [3] [4]
Developmental regression is associated with diagnoses of autism spectrum disorder, [3] childhood disintegrative disorder, [4] Rett syndrome, [5] Landau-Kleffner syndrome, [6] and neuro-degenerative diseases. [7] The loss of motor, language, and social skills can be treated with occupational therapy, [8] physical therapy, [9] and speech therapy ...
Frank R. Kleffner (October 10, 1925 – June 12, 2015) [1] was an American pathologist who was a professor at Washington University in St. Louis, noted for his contributions in the fields of speech and language pathology and hearing. His work with William Landau and Harold Klawans advanced his
William Milton Landau (October 10, 1924 [1] – November 2, 2017) was an American neurologist who was a professor of neurology at the Washington University School of Medicine in St. Louis, Missouri. [2] It was within his specialty of stroke and movement disorders that he gained eponymous recognition for the Landau–Kleffner syndrome. [2] [3]
Multiple subpial transections can help to reduce or eliminate seizures arising from vital functional areas of the cerebral cortex. This procedure has been successful in an unusual type of epilepsy called Landau-Kleffner syndrome, [1] at least for a limited time.
sleep syndrome Landau-Kleffner syndrome: Generalized and/or focal Epileptic spasms Atonic seizures Generalized tonic-clonic seizures Myoclonic seizures Cognitive symptoms Typically severe developmental delay and intellectual disability: Other symptoms Movement disorders (chorea and/or dystonia) Cortical visual impairment
Living among a small band of Neanderthals in what is now eastern Spain was a child, perhaps 6 years old, with Down syndrome, as shown in a remarkable fossil preserving traits in the inner ear ...
The disorder should be differentiated from several other conditions, especially centrotemporal spikes without seizures, centrotemporal spikes with local brain pathology, central spikes in Rett syndrome and fragile X syndrome, malignant Rolandic epilepsy, temporal lobe epilepsy and Landau-Kleffner syndrome. [citation needed]