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 
                
- Osteogenesis imperfecta
 - Heart-hand syndrome
 - Achondroplasia
 - Dysosteosclerosis
 - Fibrous dysplasia of bone
 - OBSOLETE: Peripheral dysostosis
 - Hypochondroplasia
 - Omodysplasia
 - Brachydactyly-long thumb syndrome
 - Femur-fibula-ulna complex
 - Multiple osteochondromas
 - Rhizomelic chondrodysplasia punctata type 1
 - Acromelic dysplasia
 - 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
                        
- Aicardi-Goutières syndrome
 - Kabuki syndrome
 - Achondroplasia
 - Hennekam syndrome
 - GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
 - ADNP syndrome
 - KBG syndrome
 - Rubinstein-Taybi 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
 
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Achondroplasia
 - Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
 - Non-acquired isolated growth hormone deficiency
 - Laron syndrome
 - Seckel syndrome
 - Pseudoachondroplasia
 - Silver-Russell syndrome
 - Thanatophoric dysplasia
 - FGFR3-related chondrodysplasia
 - Isolated growth hormone deficiency type III
 - Hypochondroplasia
 - Diastrophic dysplasia
 - Spondyloepiphyseal dysplasia congenita
 
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 
                
- Osteogenesis imperfecta
 - Heart-hand syndrome
 - Achondroplasia
 - Dysosteosclerosis
 - Fibrous dysplasia of bone
 - OBSOLETE: Peripheral dysostosis
 - Hypochondroplasia
 - Omodysplasia
 - Brachydactyly-long thumb syndrome
 - Femur-fibula-ulna complex
 - Multiple osteochondromas
 - Rhizomelic chondrodysplasia punctata type 1
 - Acromelic dysplasia
 - 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
                        
- Aicardi-Goutières syndrome
 - Kabuki syndrome
 - Achondroplasia
 - Hennekam syndrome
 - GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
 - ADNP syndrome
 - KBG syndrome
 - Rubinstein-Taybi 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
 
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Achondroplasia
 - Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
 - Non-acquired isolated growth hormone deficiency
 - Laron syndrome
 - Seckel syndrome
 - Pseudoachondroplasia
 - Silver-Russell syndrome
 - Thanatophoric dysplasia
 - FGFR3-related chondrodysplasia
 - Isolated growth hormone deficiency type III
 - Hypochondroplasia
 - Diastrophic dysplasia
 - Spondyloepiphyseal dysplasia congenita