EPILEPSY, BENIGN NEONATAL, NONFAMILIAL
\ˈɛpɪlˌɛpsi], \ˈɛpɪlˌɛpsi], \ˈɛ_p_ɪ_l_ˌɛ_p_s_i]\
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A condition marked by recurrent seizures that occur during the first 4-6 weeks of life despite an otherwise benign neonatal course. Autosomal dominant familial and sporadic forms have been identified. Seizures generally consist of brief episodes of tonic posturing and other movements, apnea, eye deviations, and blood pressure fluctuations. These tend to remit after the 6th week of life. The risk of developing epilepsy at an older age is moderately increased in the familial form of this disorder. (Neurologia 1996 Feb;11 (2):51-5)
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Proto Oncogene Proteins c erbB 2
- cell surface protein-tyrosine kinase that is found to be overexpressed in significant number adenocarcinomas. It has extensive homology can heterodimerize EGF EPIDERMAL GROWTH FACTOR), 3 receptor (RECEPTOR, 3) and the 4 receptor. Activation of erbB-2 receptor occurs during heterodimer formation with a ligand-bound erbB family members. EC 2.7.11.-.
Nearby Words
- epilepsy
- epilepsy, absence, atypical
- epilepsy, anterior fronto polar
- epilepsy, benign frontal, childhood
- epilepsy, benign neonatal, familial
- Epilepsy, Benign Neonatal, Nonfamilial
- epilepsy, benign psychomotor, childhood
- epilepsy, cerebral
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- epilepsy, cursive reflex (running)
- epilepsy, early childhood, myoclonic