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The symptoms variably include feelings of increased self-awareness, mental clarity, certainty, feelings of "unity with everything that exists" (including the external environment), intense positive affect, a sense of intense serenity or bliss, mystical, spiritual, or religious experiences, physical well-being, a sense of "hyper-reality", and time dilation, among others.
This is a list of major and frequently observed neurological disorders (e.g., Alzheimer's disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). There is disagreement over the definitions and criteria used to delineate various disorders and whether some of these conditions should be classified as ...
American Sign Language: United States and Canada: ASL is also officially recognized as a language in Canada due to the passage of Bill C-81, the Accessible Canada Act. Black American Sign Language is a dialect of ASL. Argentine Sign Language: Spain and Italy [citation needed] (Lengua de Señas Argentina – LSA) Bay Islands Sign Language ...
Initial symptoms include restlessness, agitation, malaise, or a fixed stare. Then comes the more characteristically described extreme and sustained upward deviation of the eyes. In addition, the eyes may converge, deviate upward and laterally, or deviate downward.
An epilepsy syndrome is defined as "a characteristic cluster of clinical and Electroencephalography (EEG) features, often supported by specific etiological findings (structural, genetic, metabolic, immune, and infectious)." [1] Syndromes are characterized by seizure types and specific findings on EEGs. Epilepsy syndromes often begin, and may ...
Diagnosis of epilepsy can be difficult. A number of other conditions may present very similar signs and symptoms to seizures, including syncope, hyperventilation, migraines, narcolepsy, panic attacks and psychogenic non-epileptic seizures (PNES). [133] [134] In particular, syncope can be accompanied by a short episode of convulsions. [135]
Ohtahara syndrome (OS), also known as Early Infantile Developmental & Epileptic Encephalopathy (EIDEE) [2] is a progressive epileptic encephalopathy.The syndrome is outwardly characterized by tonic spasms and partial seizures within the first few months of life, [3] and receives its more elaborate name from the pattern of burst activity on an electroencephalogram (EEG).
In terms of the diagnosis of adenylosuccinate lyase deficiency one should look for (or exam/method): [4] [3] Demonstration of succinylpurines in extracellular fluids like plasma , cerebrospinal fluid and/or urine using high-pressure liquid chromatography, with or without mass spectroscopy