These disorders include Awakening tonic-clonic, juvenile myoclonic epilepsy, benign rolandic epilepsy, Landau-Kleffner Syndrome (LKS), and frontal lobe epilepsy. Those already suffering from a pre-existing seizure disorder may be more prone to developing nocturnal seizures. Sedative useĬommonly used by those suffering from sleeplessness, sedatives have been known to aggravate nocturnal seizure problems. However, drinking too much coffee and therefore caffeine can be a possible trigger for nocturnal seizures. This may include stimulants such as coffee, commonly used to overcome day time drowsiness. Stress can affect the mental process of the brain which can, in turn, be a possible trigger for nocturnal seizures. A particular brain wave may trigger a nocturnal seizure Fevers and stress This is why people who are detoxifying from severe alcohol abuse are encouraged to do so in a clinic or detox facility so they are constantly under supervision Sleep deprivationĪ possible trigger for seizures especially for those who are prone to develop nocturnal seizures Changes in brain electrical activityĭuring sleep, our brain goes through several sleep stages, of which our brains channel through various electrical brain wave changes. ![]() When using substances of abuse like these, it creates a chemical shift within the brain to the point that if a person were to suddenly stop, I can lead to severe withdrawal symptoms or even seizure development. Seizure tends to develop several years after a traumatic incident. If the force striking the head is hard enough to break through the skull it can lead to massive swelling and inevitable brain damage. Bumping your head or direct blunt for trauma to the skull can violently move the brain within the skull leading to contusion (injury). While the brain is protected by the skull, injury to delicate brain tissue can still occur within it. the following are various nocturnal seizure causes: Injuries ![]() Nocturnal seizure causes can be the result of any abnormality affecting the brain and its function, some of which we don’t realize are affecting our central nervous system. The most common forms of inherited ataxia are caused by repeat expansion mutations, therefore the compre-hensive version of our panel includes repeat expansion analysis.The neural network of the brain is infinitely complex, with millions of connections making up our consciousness and controlling our daily operations. Our Ataxia / Spastic paraplegia panel is not only the best option for patients displaying gait imbalance and uncoordinated walking, but also for patients displaying spastic gait impairment, spastic weakness, and hyperreflexia or any of the combinations. ![]() However, recent information shows that these diseases share genes, pathways and mechanisms and therefore our panel covers both syndromes and involves ataxia-spasticity disease spectrum. Traditionally, ataxias and spastic paraplegia have been classified into separate categories. ![]() These disorders normally share overlapping symptoms and can only be clearly differentiated by molecular genetic testing. Our Ataxia / Spastic paraplegia panel includes genes relevant to hereditary neurological disorders characterized by ataxia and spastic paraplegia, including spinocerebellar ataxia (dominant and recessive), cerebellar ataxia, episodic ataxia, and pontocerebellar ataxia.
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