Klinik für Kinder- und Jugendmedizin am Gemeinschaftsklinikum Mittelrhein Assigned diseases:
In the following you will find the diseases that are treated in this facility:
15q13.3 microdeletion syndrome
ARX-related epileptic encephalopathy
Acquired porencephaly
Action myoclonus-renal failure syndrome
Acute disseminated encephalomyelitis
Acute encephalopathy with biphasic seizures and late reduced diffusion
Acute encephalopathy with inflammation-mediated status epilepticus
Adolescent-onset epilepsy syndrome
Adult neuronal ceroid lipofuscinosis
Aicardi syndrome
Alobar holoprosencephaly
Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome
Atypical Rett syndrome
Audiogenic seizures
Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
Autosomal dominant epilepsy with auditory features
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome
Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency
Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency
Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency
Autosomal recessive frontotemporal pachygyria
Benign adult familial myoclonic epilepsy
Benign childhood occipital epilepsy, Gastaut type
Benign childhood occipital epilepsy, Panayiotopoulos type
Benign familial infantile epilepsy
Benign familial mesial temporal lobe epilepsy
Benign familial neonatal epilepsy
Benign familial neonatal-infantile seizures
Benign focal seizures of adolescence
Benign idiopathic neonatal seizures
Benign infantile focal epilepsy with midline spikes and waves during sleep
Benign infantile seizures associated with mild gastroenteritis
Benign non-familial infantile seizures
Benign occipital epilepsy
Benign partial epilepsy of infancy with complex partial seizures
Benign partial epilepsy with secondarily generalized seizures in infancy
Benign partial infantile seizures
Bilateral frontal polymicrogyria
Bilateral frontoparietal polymicrogyria
Bilateral generalized polymicrogyria
Bilateral parasagittal parieto-occipital polymicrogyria
Bilateral perisylvian polymicrogyria
Bilateral polymicrogyria
CLN1 disease
CLN10 disease
CLN11 disease
CLN13 disease
CLN2 disease
CLN4A disease
CLN4B disease
CLN5 disease
CLN6 disease
CLN7 disease
CLN8 disease
CLN9 disease
CNTNAP2-related developmental and epileptic encephalopathy
Celiac disease-epilepsy-cerebral calcification syndrome
Central bilateral macrogyria
Cerebral cortical dysplasia
Cerebral diseases of vascular origin with epilepsy
Cerebral malformation with epilepsy
Channelopathy with epilepsy
Childhood absence epilepsy
Childhood-onset epilepsy syndrome
Chromosomal anomaly with epilepsy as a major feature
Classic paraneoplastic limbic encephalitis
Colorado tick fever
Congenital neuronal ceroid lipofuscinosis
Congenital rubella syndrome
Congenital toxoplasmosis
Constitutional megaloblastic anemia with severe neurologic disease
Continuous spikes and waves during sleep
Corpus callosum agenesis-abnormal genitalia syndrome
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Cryptogenic late-onset epileptic spasms
Cystic fibrosis
DEND syndrome
Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome
Dravet syndrome
EAST syndrome
Early infantile epileptic encephalopathy
Early myoclonic encephalopathy
Early-onset Lafora body disease
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome
Early-onset progressive encephalopathy with migrant continuous myoclonus
Eastern equine encephalitis
Eating reflex epilepsy
Encephalitis lethargica
Epilepsy syndrome
Epilepsy with eyelid myoclonia
Epilepsy with myoclonic absences
Epilepsy-telangiectasia syndrome
Epileptic encephalopathy with global cerebral demyelination
Familial encephalopathy with neuroserpin inclusion bodies
Familial focal epilepsy with variable foci
Familial infantile myoclonic epilepsy
Familial mesial temporal lobe epilepsy with febrile seizures
Familial partial epilepsy
Familial porencephaly
Familial temporal lobe epilepsy
Febrile infection-related epilepsy syndrome
Female restricted epilepsy with intellectual disability
Fetal cytomegalovirus syndrome
Focal epilepsy-intellectual disability-cerebro-cerebellar malformation
Generalized epilepsy with febrile seizures-plus
Generalized epilepsy-paroxysmal dyskinesia syndrome
Hemimegalencephaly
Hereditary neurocutaneous malformation
Herpes simplex virus encephalitis
Holoprosencephaly
Hot water reflex epilepsy
Hyper-beta-alaninemia
Hyperekplexia-epilepsy syndrome
Hypothalamic hamartomas with gelastic seizures
Idiopathic hemiconvulsion-hemiplegia syndrome
Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes
Incontinentia pigmenti
Infantile convulsions and choreoathetosis
Infantile epilepsy syndrome
Infantile epileptic-dyskinetic encephalopathy
Infantile neuronal ceroid lipofuscinosis
Infantile spasms syndrome
Infantile spasms-broad thumbs syndrome
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Infectious disease with epilepsy
Inflammatory and autoimmune disease with epilepsy
Intermediate DEND syndrome
Isolated focal cortical dysplasia
Isolated focal cortical dysplasia type I
Isolated focal cortical dysplasia type II
Ito hypomelanosis
Japanese encephalitis
Juvenile absence epilepsy
Juvenile myoclonic epilepsy
Juvenile neuronal ceroid lipofuscinosis
KDM5C-related syndromic X-linked intellectual disability
Kleefstra syndrome due to 9q34 microdeletion
Klüver-Bucy syndrome
La Crosse encephalitis
Lafora disease
Landau-Kleffner syndrome
Late infantile neuronal ceroid lipofuscinosis
Lennox-Gastaut syndrome
Limbic encephalitis
Limbic encephalitis associated with antibodies to cell membrane antigens
Limbic encephalitis with DPP6 antibodies
Limbic encephalitis with LGI1 antibodies
Limbic encephalitis with caspr2 antibodies
Limbic encephalitis with nCMAgs antibodies
Lissencephaly
Lobar holoprosencephaly
MERRF
Malignant migrating focal seizures of infancy
Meningococcal meningitis
Mesial temporal lobe epilepsy with hippocampal sclerosis
Metabolic diseases with epilepsy
Microform holoprosencephaly
Microlissencephaly-micromelia syndrome
Micturation-induced seizures
Midline interhemispheric variant of holoprosencephaly
Monogenic disease with epilepsy
Morvan syndrome
Moynahan syndrome
Mycoplasma encephalitis
Myoclonic epilepsy in non-progressive encephalopathies
Myoclonic epilepsy of infancy
Myoclonic-astatic epilepsy
NMDA receptor encephalitis
Neonatal epilepsy syndrome
Neuroectodermal melanolysosomal disease
New-onset refractory status epilepticus
Nodular neuronal heterotopia
Non-herpetic acute limbic encephalitis
Non-paraneoplastic limbic encephalitis
Non-syndromic cerebral malformation due to abnormal neuronal migration
OBSOLETE: CLN3 disease
Occipital pachygyria and polymicrogyria
Oculocerebrocutaneous syndrome
Orgasm-induced seizures
PEHO syndrome
PEHO-like syndrome
Pachygyria-intellectual disability-epilepsy syndrome
Paraneoplastic limbic encephalitis
Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome
Partington syndrome
Perioral myoclonia with absences
Periventricular nodular heterotopia
Photosensitive epilepsy
Pneumococcal meningitis
Polymicrogyria
Porencephaly
Posttransplant acute limbic encephalitis
Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome
Progressive epilepsy-intellectual disability syndrome, Finnish type
Progressive hemifacial atrophy
Progressive myoclonic epilepsy
Progressive myoclonic epilepsy type 1
Progressive myoclonic epilepsy type 3
Progressive myoclonic epilepsy type 5
Progressive myoclonic epilepsy type 6
Progressive myoclonic epilepsy with dystonia
Proteus syndrome
Rare epilepsy
Rasmussen subacute encephalitis
Reading seizures
Reflex epilepsy
Rett syndrome
Ring chromosome 14 syndrome
Ring chromosome 20 syndrome
Rolandic epilepsy
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
Rolandic epilepsy-speech dyspraxia syndrome
Rubella panencephalitis
Schizencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Severe neonatal-onset encephalopathy with microcephaly
Solitary median maxillary central incisor syndrome
St. Louis encephalitis
Startle epilepsy
Sturge-Weber syndrome
Sub-cortical nodular heterotopia
Subacute sclerosing leukoencephalitis
Subcortical band heterotopia
Subependymal nodular heterotopia
Thiamine-responsive encephalopathy
Thinking seizures
Tick-borne encephalitis
Tuberous sclerosis complex
Unilateral focal polymicrogyria
Unilateral hemispheric polymicrogyria
Unilateral polymicrogyria
W syndrome
West-Nile encephalitis
Western equine encephalitis
X-linked dominant intellectual disability-epilepsy syndrome
X-linked epilepsy-learning disabilities-behavior disorders syndrome
X-linked intellectual disability, Hedera type
X-linked intellectual disability-epilepsy syndrome
X-linked lissencephaly with abnormal genitalia
X-linked spasticity-intellectual disability-epilepsy syndrome