Skeletal dysplasia-epilepsy-short stature syndrome
All Entries 3
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Uniklinik Köln Centrum für Seltene Erkrankungen Köln (CESEK)
                    Kerpener Straße 62
                    50937 Köln 
                
- Brachydactyly-long thumb syndrome
 - Omodysplasia
 - Rhizomelic chondrodysplasia punctata type 1
 - Multiple osteochondromas
 - Dysosteosclerosis
 - Heart-hand syndrome
 - Femur-fibula-ulna complex
 - OBSOLETE: Peripheral dysostosis
 - Fibrous dysplasia of bone
 - Hypochondroplasia
 - Achondroplasia
 - Acromelic dysplasia
 - Osteogenesis imperfecta
 - Metachondromatosis
 - Paralytic facial malformation
 
Zentrum für seltene Entwicklungsstörungen am kbo-Kinderzentrum München
Zentrum für Seltene Erkrankungen am Klinikum rechts der Isar der Technischen Universität München Klinikum rechts der Isar der Technischen Universität München
                    Heiglhofstr. 65
                    81377 München
                
                             089 710090
                            
 089 71009253
                            
                                
 Website
                            
                            
 Email
                        
- 22q11.2 deletion syndrome
 - Achondroplasia
 - Hennekam syndrome
 - KBG syndrome
 - Kabuki syndrome
 - Aicardi-Goutières syndrome
 - ADNP syndrome
 - GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
 - Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
 - Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
 - Infantile spasms syndrome
 - Rubinstein-Taybi syndrome
 
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Non-acquired isolated growth hormone deficiency
 - Spondyloepiphyseal dysplasia congenita
 - Seckel syndrome
 - Pseudoachondroplasia
 - Isolated growth hormone deficiency type III
 - Hypochondroplasia
 - Laron syndrome
 - Achondroplasia
 - Silver-Russell syndrome
 - Thanatophoric dysplasia
 - Diastrophic dysplasia
 - Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
 - FGFR3-related chondrodysplasia
 
Parent facilities 0
Genetic Advices 0
Care facilities 2
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Uniklinik Köln Centrum für Seltene Erkrankungen Köln (CESEK)
                    Kerpener Straße 62
                    50937 Köln 
                
- Brachydactyly-long thumb syndrome
 - Omodysplasia
 - Rhizomelic chondrodysplasia punctata type 1
 - Multiple osteochondromas
 - Dysosteosclerosis
 - Heart-hand syndrome
 - Femur-fibula-ulna complex
 - OBSOLETE: Peripheral dysostosis
 - Fibrous dysplasia of bone
 - Hypochondroplasia
 - Achondroplasia
 - Acromelic dysplasia
 - Osteogenesis imperfecta
 - Metachondromatosis
 - Paralytic facial malformation
 
Zentrum für seltene Entwicklungsstörungen am kbo-Kinderzentrum München
Zentrum für Seltene Erkrankungen am Klinikum rechts der Isar der Technischen Universität München Klinikum rechts der Isar der Technischen Universität München
                    Heiglhofstr. 65
                    81377 München
                
                             089 710090
                            
 089 71009253
                            
                                
 Website
                            
                            
 Email
                        
- 22q11.2 deletion syndrome
 - Achondroplasia
 - Hennekam syndrome
 - KBG syndrome
 - Kabuki syndrome
 - Aicardi-Goutières syndrome
 - ADNP syndrome
 - GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
 - Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
 - Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
 - Infantile spasms syndrome
 - Rubinstein-Taybi syndrome
 
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Non-acquired isolated growth hormone deficiency
 - Spondyloepiphyseal dysplasia congenita
 - Seckel syndrome
 - Pseudoachondroplasia
 - Isolated growth hormone deficiency type III
 - Hypochondroplasia
 - Laron syndrome
 - Achondroplasia
 - Silver-Russell syndrome
 - Thanatophoric dysplasia
 - Diastrophic dysplasia
 - Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
 - FGFR3-related chondrodysplasia