Epilepsy, Benign Neonatal [epilepsie benigní neonatální]

topical
13
Terms

benigní familiární infantilní záchvaty
benigní familiární novorozenecké křeče
benigní neonatální epilepsie familiární
benigní neonatální epilepsie nefamiliární
benigní non-familiární neonatální záchvaty
benigní novorozenecké křeče
familiární benigní křeče infantilní
familiární benigní neonatální epilepsie
nefamiliární benigní neonatální epilepsie
novorozenecké křeče benigní

 

Benign Familial Infantile Convulsions
Benign Familial Infantile Convulsions Syndrome
Benign Familial Neonatal Convulsions
Benign Familial Neonatal Epilepsy
Benign Familial Neonatal-Infantile Seizures
Benign Infantile Familial Convulsions
Benign Neonatal Convulsions
Benign Neonatal Epilepsy
Benign Neonatal Epilepsy, Nonfamilial
Benign Neonatal Non-Familial Convulsions
Benign Neonatal Nonfamilial Epilepsy
Benign Non-Familial Neonatal Convulsions
Convulsions Benign Familial Neonatal
Convulsions, Benign Familial Infantile, 1
Convulsions, Benign Familial Infantile, 3
Convulsions, Benign Neonatal, Familial
Convulsions, Benign Neonatal, Non-Familial
Epilepsy, Benign Neonatal-Infantile
Epilepsy, Benign Neonatal, Familial
Epilepsy, Benign Neonatal, Non-Familial
Epilepsy, Benign Neonatal, Nonfamilial
Familial Benign Neonatal Convulsions
Familial Benign Neonatal Epilepsy
Neonatal Convulsions, Benign
Non-Familial Benign Neonatal Convulsions
Non-Familial Benign Neonatal Epilepsy
Seizures, Benign Familial Infantile, 1
Seizures, Benign Familial Infantile, 3
Seizures, Benign Familial Neonatal-Infantile

Persistent link   https://www.medvik.cz/link/D020936
Definition

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)

DUI
D020936 MeSH Browser
CUI
M0328386
Previous indexing
Epilepsy (1968-1999)
History note
2000
Public note
2000

C Diseases
C10.228.140 Brain Diseases 1 177
C10.228.140.490 Epilepsy 3 247
C10.228.140.490.125 Drug Resistant Epilepsy 117
C10.228.140.490.360 Epilepsies, Partial 193
C10.228.140.490.370 Epilepsy, Benign Neonatal 13
C10.228.140.490.375 Epilepsy, Generalized 58
C10.228.140.490.380 Epilepsy, Post-Traumatic 46
C10.228.140.490.450 Epilepsy, Reflex 22
C10.228.140.490.493 Epileptic Syndromes 19
C16.614.053 Anemia, Neonatal 22
C16.614.092 Asphyxia Neonatorum 172
C16.614.131 Birth Injuries 158
C16.614.166 Colic 125
C16.614.213 Cystic Fibrosis 1 328
C16.614.378 Hernia, Umbilical 45
C16.614.438 Hydrophthalmos 9
C16.614.492 Ichthyosis 62
C16.614.595 Mobius Syndrome 10
C16.614.627 Neonatal Sepsis 35
C16.614.660 OEIS Complex
C16.614.810 Sclerema Neonatorum 2
C16.614.868 Syphilis, Congenital 87
C16.614.947 Wolman Disease 15