Short stature, Brussels type
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
- Heart-hand syndrome
- Achondroplasia
- Dysosteosclerosis
- OBSOLETE: Peripheral dysostosis
- Brachydactyly-long thumb syndrome
- Fibrous dysplasia of bone
- Hypochondroplasia
- Femur-fibula-ulna complex
- Acromelic dysplasia
- Multiple osteochondromas
- Rhizomelic chondrodysplasia punctata type 1
- Omodysplasia
- Osteogenesis imperfecta
- Metachondromatosis
- Paralytic facial malformation
Bundesselbsthilfeverband Kleinwüchsiger Menschen e.V. (VKM)
Steinheimer Str. 26
74354
Besigheim
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
- Isolated growth hormone deficiency type III
- Hypochondroplasia
- Laron syndrome
- FGFR3-related chondrodysplasia
- 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
- Achondroplasia
- Dysosteosclerosis
- OBSOLETE: Peripheral dysostosis
- Brachydactyly-long thumb syndrome
- Fibrous dysplasia of bone
- Hypochondroplasia
- Femur-fibula-ulna complex
- Acromelic dysplasia
- Multiple osteochondromas
- Rhizomelic chondrodysplasia punctata type 1
- Omodysplasia
- Osteogenesis imperfecta
- Metachondromatosis
- Paralytic facial malformation
Supportgroups 2
Bundesselbsthilfeverband Kleinwüchsiger Menschen e.V. (VKM)
Steinheimer Str. 26
74354
Besigheim
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
- Isolated growth hormone deficiency type III
- Hypochondroplasia
- Laron syndrome
- FGFR3-related chondrodysplasia
- Seckel syndrome
- Pseudoachondroplasia