KCNQ2-related epileptic encephalopathy
All Entries 4
HELIOS Klinikum Erfurt
Nordhäuser Straße 74
99089 Erfurt
- Full NF2-related schwannomatosis
- Juvenile idiopathic arthritis
- Rare skin tumor or hamartoma
- Wilson disease
- Arnold-Chiari malformation type II
- Unexplained long-lasting fever/inflammatory syndrome
- Arnold-Chiari malformation type I
- Cystic fibrosis
- Myasthenia gravis
- Syringomyelia
- Neurofibromatosis type 1
Epilepsiezentrum Frankfurt Rhein-Main am Universitätsklinikum Frankfurt
Universitätsklinikum Frankfurt Frankfurter Referenzzentrum für Seltene Erkrankungen (FRZSE)
Schleusenweg 2 – 16
60528 Frankfurt
069 630185065
069 63017075
Website
Email
Kleinwachau Sächsisches Epilepsiezentrum Radeberg
Wachauer Straße 30
01454 Radeberg
- Chromosomal anomaly with epilepsy as a major feature
- Metal transport or utilization disorder with epilepsy
- Cerebral diseases of vascular origin with epilepsy
- Infantile epilepsy syndrome
- Metabolic diseases with epilepsy
- Other metabolic disease with epilepsy
- ARX-related epileptic encephalopathy
- Cerebral malformation with epilepsy
- Neonatal epilepsy syndrome
- Childhood absence epilepsy
- Epilepsy-telangiectasia syndrome
- Startle epilepsy
- Infantile spasms syndrome
- Audiogenic seizures
Parent facilities 0
Genetic Advices 0
Care facilities 3
HELIOS Klinikum Erfurt
Nordhäuser Straße 74
99089 Erfurt
- Full NF2-related schwannomatosis
- Juvenile idiopathic arthritis
- Rare skin tumor or hamartoma
- Wilson disease
- Arnold-Chiari malformation type II
- Unexplained long-lasting fever/inflammatory syndrome
- Arnold-Chiari malformation type I
- Cystic fibrosis
- Myasthenia gravis
- Syringomyelia
- Neurofibromatosis type 1
Epilepsiezentrum Frankfurt Rhein-Main am Universitätsklinikum Frankfurt
Universitätsklinikum Frankfurt Frankfurter Referenzzentrum für Seltene Erkrankungen (FRZSE)
Schleusenweg 2 – 16
60528 Frankfurt
069 630185065
069 63017075
Website
Email
Kleinwachau Sächsisches Epilepsiezentrum Radeberg
Wachauer Straße 30
01454 Radeberg
- Chromosomal anomaly with epilepsy as a major feature
- Metal transport or utilization disorder with epilepsy
- Cerebral diseases of vascular origin with epilepsy
- Infantile epilepsy syndrome
- Metabolic diseases with epilepsy
- Other metabolic disease with epilepsy
- ARX-related epileptic encephalopathy
- Cerebral malformation with epilepsy
- Neonatal epilepsy syndrome
- Childhood absence epilepsy
- Epilepsy-telangiectasia syndrome
- Startle epilepsy
- Infantile spasms syndrome
- Audiogenic seizures