Short stature-deafness-neutrophil dysfunction-dysmorphism 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
- Osteogenesis imperfecta
- Fibrous dysplasia of bone
- Metachondromatosis
- Heart-hand syndrome
- Acromelic dysplasia
- Multiple osteochondromas
- Achondroplasia
- Brachydactyly-long thumb syndrome
- Omodysplasia
- Femur-fibula-ulna complex
- Hypochondroplasia
- OBSOLETE: Peripheral dysostosis
- Paralytic facial malformation
- Dysosteosclerosis
- Rhizomelic chondrodysplasia punctata type 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Diastrophic dysplasia
- Silver-Russell syndrome
- Non-acquired isolated growth hormone deficiency
- Thanatophoric dysplasia
- Spondyloepiphyseal dysplasia congenita
- Hypochondroplasia
- Isolated growth hormone deficiency type III
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Laron syndrome
- Achondroplasia
- FGFR3-related chondrodysplasia
- Pseudoachondroplasia
- Seckel syndrome
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
- Osteogenesis imperfecta
- Fibrous dysplasia of bone
- Metachondromatosis
- Heart-hand syndrome
- Acromelic dysplasia
- Multiple osteochondromas
- Achondroplasia
- Brachydactyly-long thumb syndrome
- Omodysplasia
- Femur-fibula-ulna complex
- Hypochondroplasia
- OBSOLETE: Peripheral dysostosis
- Paralytic facial malformation
- Dysosteosclerosis
- Rhizomelic chondrodysplasia punctata type 1
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Diastrophic dysplasia
- Silver-Russell syndrome
- Non-acquired isolated growth hormone deficiency
- Thanatophoric dysplasia
- Spondyloepiphyseal dysplasia congenita
- Hypochondroplasia
- Isolated growth hormone deficiency type III
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Laron syndrome
- Achondroplasia
- FGFR3-related chondrodysplasia
- Pseudoachondroplasia
- Seckel syndrome