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  2. Epilepsy in children - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_in_children

    The epileptic seizure in the vast majority of pediatric epilepsy patients is ephemeral, and symptoms typically subside on their own after the seizure comes to an end, but some children experience what is known as a “seizure cluster," in which the first seizure is followed by a second episode approximately six hours later.

  3. Phenytoin - Wikipedia

    en.wikipedia.org/wiki/Phenytoin

    Phenytoin (PHT), sold under the brand name Dilantin among others, [1] is an anti-seizure medication. [3] It is useful for the prevention of tonic-clonic seizures (also known as grand mal seizures) and focal seizures, but not absence seizures. [3]

  4. Epilepsy and pregnancy - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_and_pregnancy

    For most patients with epilepsy, the risk of passing the disease to a child is only slightly higher than the risk of a member of the general population having a child with epilepsy (1–2%). Specifically, the hereditary rates for patients with: Any type of epilepsy is 3.5–6%; Focal epilepsy is 1–5%; Generalized epilepsy is 6–8%. [5]

  5. Anticonvulsant - Wikipedia

    en.wikipedia.org/wiki/Anticonvulsant

    Similarly, children exposed lamotrigine or phenytoin in the womb do not seem to differ in their skills compared to those who were exposed to carbamazepine. [96] There is inadequate evidence to determine if newborns of women with epilepsy taking anticonvulsants have a substantially increased risk of hemorrhagic disease of the newborn. [94]

  6. Fosphenytoin - Wikipedia

    en.wikipedia.org/wiki/Fosphenytoin

    Fosphenytoin is approved in the United States for the short-term (five days or fewer) treatment of epilepsy when more widely used means of phenytoin administration are not possible or are ill-advised, [4] such as endotracheal intubation, status epilepticus or some other type of repeated seizures; cluster seizure, vomiting, and/or the patient is unalert or not awake or both.

  7. Rolandic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Rolandic_epilepsy

    Benign Rolandic epilepsy or self-limited epilepsy with centrotemporal spikes (formerly benign childhood epilepsy with centrotemporal spikes (BECTS)) is the most common epilepsy syndrome in childhood. [ 1 ] [ 2 ] Most children will outgrow the syndrome (it starts around the age of 3–13 with a peak around 8–9 years and stops around age 14 ...

  8. Causes of seizures - Wikipedia

    en.wikipedia.org/wiki/Causes_of_seizures

    In children between the ages of 6 months and 5 years, a fever of 38 °C (100.4 °F) or higher may lead to a febrile seizure. [25] About 2-5% of all children will experience such a seizure during their childhood. [26] In most cases, a febrile seizure will not indicate epilepsy. [26]

  9. Fetal hydantoin syndrome - Wikipedia

    en.wikipedia.org/wiki/Fetal_hydantoin_syndrome

    Dilantin is the brand name of the drug phenytoin sodium in the United States, commonly used in the treatment of epilepsy. It may also be called congenital hydantoin syndrome, [1] fetal hydantoin syndrome, dilantin embryopathy, or phenytoin embryopathy. Association with EPHX1 has been suggested. [2]

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