Epilepsy-microcephaly-skeletal dysplasia syndrome
Parent facilities 0
Genetic Advices 1
Institut für Medizinische Genetik und Humangenetik an der Charité Berlin
Berliner Centrum für Seltene Erkrankungen (BCSE) Charité Universitätsmedizin Berlin
Augustenburger Platz 1
13353 Berlin
030 450569122
030 450569915
Website
Care facilities 2
Zentrum für seltene Entwicklungsstörungen am kbo-Kinderzentrum München
Klinikum rechts der Isar der Technischen Universität München Zentrum für Seltene Erkrankungen am Klinikum rechts der Isar der Technischen Universität München
Heiglhofstr. 65
81377 München
089 710090
089 71009253
Website
Email
- GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
- KBG syndrome
- ADNP syndrome
- Kabuki syndrome
- Achondroplasia
- 22q11.2 deletion syndrome
- Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
- Rubinstein-Taybi syndrome
- Infantile spasms syndrome
- Aicardi-Goutières syndrome
- Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
- Hennekam syndrome
Kleinwachau Sächsisches Epilepsiezentrum Radeberg
Wachauer Straße 30
01454 Radeberg
- Cerebral malformation with epilepsy
- Audiogenic seizures
- Startle epilepsy
- Childhood absence epilepsy
- Infantile spasms syndrome
- Epilepsy-telangiectasia syndrome
- Chromosomal anomaly with epilepsy as a major feature
- Cerebral diseases of vascular origin with epilepsy
- Metal transport or utilization disorder with epilepsy
- Other metabolic disease with epilepsy
- ARX-related epileptic encephalopathy
- Infantile epilepsy syndrome
- Metabolic diseases with epilepsy
- Neonatal epilepsy syndrome