Short stature-wormian bones-dextrocardia syndrome
All Entries 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 
                
- Heart-hand syndrome
 - OBSOLETE: Peripheral dysostosis
 - Metachondromatosis
 - Fibrous dysplasia of bone
 - Brachydactyly-long thumb syndrome
 - Osteogenesis imperfecta
 - Rhizomelic chondrodysplasia punctata type 1
 - Acromelic dysplasia
 - Dysosteosclerosis
 - Femur-fibula-ulna complex
 - Paralytic facial malformation
 - Hypochondroplasia
 - Multiple osteochondromas
 - Omodysplasia
 - Achondroplasia
 
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Non-acquired isolated growth hormone deficiency
 - Silver-Russell syndrome
 - Achondroplasia
 - Spondyloepiphyseal dysplasia congenita
 - Diastrophic dysplasia
 - Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
 - Thanatophoric dysplasia
 - Hypochondroplasia
 - FGFR3-related chondrodysplasia
 - Isolated growth hormone deficiency type III
 - Laron syndrome
 - Seckel syndrome
 - Pseudoachondroplasia
 
Parent facilities 0
Genetic Advices 0
Care facilities 1
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Uniklinik Köln Centrum für Seltene Erkrankungen Köln (CESEK)
                    Kerpener Straße 62
                    50937 Köln 
                
- Heart-hand syndrome
 - OBSOLETE: Peripheral dysostosis
 - Metachondromatosis
 - Fibrous dysplasia of bone
 - Brachydactyly-long thumb syndrome
 - Osteogenesis imperfecta
 - Rhizomelic chondrodysplasia punctata type 1
 - Acromelic dysplasia
 - Dysosteosclerosis
 - Femur-fibula-ulna complex
 - Paralytic facial malformation
 - Hypochondroplasia
 - Multiple osteochondromas
 - Omodysplasia
 - Achondroplasia
 
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
                    
                        
                        
                            Leinestraße 2
                        
                    
                    
                        
                        
                            28199
                        
                    
                    Bremen
                
- Non-acquired isolated growth hormone deficiency
 - Silver-Russell syndrome
 - Achondroplasia
 - Spondyloepiphyseal dysplasia congenita
 - Diastrophic dysplasia
 - Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
 - Thanatophoric dysplasia
 - Hypochondroplasia
 - FGFR3-related chondrodysplasia
 - Isolated growth hormone deficiency type III
 - Laron syndrome
 - Seckel syndrome
 - Pseudoachondroplasia