Rare bone disease
All Entries 2
Altonaer Kinderkrankenhaus
Bleickenallee 38
22763 Hamburg
040 889080
040 88908366
Website
Email
- Osteogenesis imperfecta
- 22q11.2 deletion syndrome
- Neurocutaneous melanocytosis
- Autosomal dominant polycystic kidney disease
- Large congenital melanocytic nevus
- Diaphragmatic or abdominal wall malformation
- Neural tube defect
- Digestive tract malformation
- Autosomal recessive polycystic kidney disease
- Rare bone disease
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Non-acquired isolated growth hormone deficiency
- Thanatophoric dysplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Diastrophic dysplasia
- Spondyloepiphyseal dysplasia congenita
- Hypochondroplasia
- Isolated growth hormone deficiency type III
- Pseudoachondroplasia
- FGFR3-related chondrodysplasia
- Silver-Russell syndrome
- Achondroplasia
- Laron syndrome
- Seckel syndrome
Parent facilities 0
Genetic Advices 0
Care facilities 1
Altonaer Kinderkrankenhaus
Bleickenallee 38
22763 Hamburg
040 889080
040 88908366
Website
Email
- Osteogenesis imperfecta
- 22q11.2 deletion syndrome
- Neurocutaneous melanocytosis
- Autosomal dominant polycystic kidney disease
- Large congenital melanocytic nevus
- Diaphragmatic or abdominal wall malformation
- Neural tube defect
- Digestive tract malformation
- Autosomal recessive polycystic kidney disease
- Rare bone disease
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Non-acquired isolated growth hormone deficiency
- Thanatophoric dysplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Diastrophic dysplasia
- Spondyloepiphyseal dysplasia congenita
- Hypochondroplasia
- Isolated growth hormone deficiency type III
- Pseudoachondroplasia
- FGFR3-related chondrodysplasia
- Silver-Russell syndrome
- Achondroplasia
- Laron syndrome
- Seckel syndrome