Parastremmatic dwarfism
All Entries 4
Altonaer Kinderkrankenhaus
Bleickenallee 38
22763 Hamburg
040 889080
040 88908366
Website
Email
- Rare bone disease
- Diaphragmatic or abdominal wall malformation
- Autosomal recessive polycystic kidney disease
- 22q11.2 deletion syndrome
- Digestive tract malformation
- Large congenital melanocytic nevus
- Neural tube defect
- Neurocutaneous melanocytosis
- Autosomal dominant polycystic kidney disease
- Osteogenesis imperfecta
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Centrum für Seltene Erkrankungen Köln (CESEK) Uniklinik Köln
Kerpener Straße 62
50937 Köln
- Dysosteosclerosis
- Paralytic facial malformation
- Hypochondroplasia
- Femur-fibula-ulna complex
- Osteogenesis imperfecta
- Multiple osteochondromas
- Omodysplasia
- Acromelic dysplasia
- Achondroplasia
- Rhizomelic chondrodysplasia punctata type 1
- Metachondromatosis
- Heart-hand syndrome
- OBSOLETE: Peripheral dysostosis
- Fibrous dysplasia of bone
- Brachydactyly-long thumb syndrome
Bundesselbsthilfeverband Kleinwüchsiger Menschen e.V. (VKM)
Steinheimer Str. 26
74354
Besigheim
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Pseudoachondroplasia
- Thanatophoric dysplasia
- Spondyloepiphyseal dysplasia congenita
- Isolated growth hormone deficiency type III
- Hypochondroplasia
- Seckel syndrome
- Non-acquired isolated growth hormone deficiency
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Laron syndrome
- Diastrophic dysplasia
- Silver-Russell syndrome
- Achondroplasia
- FGFR3-related chondrodysplasia
Parent facilities 0
Genetic Advices 0
Care facilities 2
Altonaer Kinderkrankenhaus
Bleickenallee 38
22763 Hamburg
040 889080
040 88908366
Website
Email
- Rare bone disease
- Diaphragmatic or abdominal wall malformation
- Autosomal recessive polycystic kidney disease
- 22q11.2 deletion syndrome
- Digestive tract malformation
- Large congenital melanocytic nevus
- Neural tube defect
- Neurocutaneous melanocytosis
- Autosomal dominant polycystic kidney disease
- Osteogenesis imperfecta
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Centrum für Seltene Erkrankungen Köln (CESEK) Uniklinik Köln
Kerpener Straße 62
50937 Köln
- Dysosteosclerosis
- Paralytic facial malformation
- Hypochondroplasia
- Femur-fibula-ulna complex
- Osteogenesis imperfecta
- Multiple osteochondromas
- Omodysplasia
- Acromelic dysplasia
- Achondroplasia
- Rhizomelic chondrodysplasia punctata type 1
- Metachondromatosis
- Heart-hand syndrome
- OBSOLETE: Peripheral dysostosis
- Fibrous dysplasia of bone
- Brachydactyly-long thumb syndrome
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
- Pseudoachondroplasia
- Thanatophoric dysplasia
- Spondyloepiphyseal dysplasia congenita
- Isolated growth hormone deficiency type III
- Hypochondroplasia
- Seckel syndrome
- Non-acquired isolated growth hormone deficiency
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Laron syndrome
- Diastrophic dysplasia
- Silver-Russell syndrome
- Achondroplasia
- FGFR3-related chondrodysplasia