Skeletal dysplasia-epilepsy-short stature syndrome
All Entries 3
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Centrum für Seltene Erkrankungen Köln (CESEK) Uniklinik Köln
                    Kerpener Straße 62
                    50937 Köln 
                
- Dysosteosclerosis
 - Acromelic dysplasia
 - Multiple osteochondromas
 - Achondroplasia
 - Brachydactyly-long thumb syndrome
 - Femur-fibula-ulna complex
 - Fibrous dysplasia of bone
 - Hypochondroplasia
 - OBSOLETE: Peripheral dysostosis
 - Heart-hand syndrome
 - Rhizomelic chondrodysplasia punctata type 1
 - Osteogenesis imperfecta
 - Omodysplasia
 - Metachondromatosis
 - Paralytic facial malformation
 
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
                        
- KBG syndrome
 - Kabuki syndrome
 - Achondroplasia
 - Hennekam syndrome
 - ADNP syndrome
 - Infantile spasms syndrome
 - Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
 - Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
 - 22q11.2 deletion syndrome
 - Rubinstein-Taybi syndrome
 - Aicardi-Goutières syndrome
 - GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
 
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Hypochondroplasia
 - FGFR3-related chondrodysplasia
 - Isolated growth hormone deficiency type III
 - Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
 - Pseudoachondroplasia
 - Thanatophoric dysplasia
 - Spondyloepiphyseal dysplasia congenita
 - Non-acquired isolated growth hormone deficiency
 - Diastrophic dysplasia
 - Seckel syndrome
 - Achondroplasia
 - Silver-Russell syndrome
 - Laron syndrome
 
Parent facilities 0
Genetic Advices 0
Care facilities 2
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Centrum für Seltene Erkrankungen Köln (CESEK) Uniklinik Köln
                    Kerpener Straße 62
                    50937 Köln 
                
- Dysosteosclerosis
 - Acromelic dysplasia
 - Multiple osteochondromas
 - Achondroplasia
 - Brachydactyly-long thumb syndrome
 - Femur-fibula-ulna complex
 - Fibrous dysplasia of bone
 - Hypochondroplasia
 - OBSOLETE: Peripheral dysostosis
 - Heart-hand syndrome
 - Rhizomelic chondrodysplasia punctata type 1
 - Osteogenesis imperfecta
 - Omodysplasia
 - Metachondromatosis
 - Paralytic facial malformation
 
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
                        
- KBG syndrome
 - Kabuki syndrome
 - Achondroplasia
 - Hennekam syndrome
 - ADNP syndrome
 - Infantile spasms syndrome
 - Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
 - Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
 - 22q11.2 deletion syndrome
 - Rubinstein-Taybi syndrome
 - Aicardi-Goutières syndrome
 - GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
 
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Hypochondroplasia
 - FGFR3-related chondrodysplasia
 - Isolated growth hormone deficiency type III
 - Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
 - Pseudoachondroplasia
 - Thanatophoric dysplasia
 - Spondyloepiphyseal dysplasia congenita
 - Non-acquired isolated growth hormone deficiency
 - Diastrophic dysplasia
 - Seckel syndrome
 - Achondroplasia
 - Silver-Russell syndrome
 - Laron syndrome