Léri-Weill dyschondrosteosis
All Entries 3
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Centrum für Seltene Erkrankungen Köln (CESEK) Uniklinik Köln
Kerpener Straße 62
50937 Köln
- Fibrous dysplasia of bone
- Osteogenesis imperfecta
- Heart-hand syndrome
- Achondroplasia
- Omodysplasia
- Acromelic dysplasia
- Metachondromatosis
- Paralytic facial malformation
- Multiple osteochondromas
- Femur-fibula-ulna complex
- Rhizomelic chondrodysplasia punctata type 1
- Dysosteosclerosis
- OBSOLETE: Peripheral dysostosis
- Hypochondroplasia
- Brachydactyly-long thumb syndrome
Zentrum für Seltene Endokrine Erkrankungen (hormonelle Erkrankungen) am Universitätsklinikum Ulm
Universitätsklinikum Ulm Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm
Eythstraße 24
89075 Ulm
0731 50057401
0731 50057407
Website
Email
- Primary lipodystrophy
- Central diabetes insipidus
- Pseudohypoparathyroidism type 1A
- Rare diabetes mellitus
- Craniopharyngioma
- Multiple endocrine neoplasia
- Genetic obesity
- Congenital hypogonadotropic hypogonadism
- Addison disease
- Congenital isolated hyperinsulinism
- Prolactinoma
- Acquired lipodystrophy
- Acromegaly
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Spondyloepiphyseal dysplasia congenita
- Diastrophic dysplasia
- Silver-Russell syndrome
- Thanatophoric dysplasia
- Seckel syndrome
- Non-acquired isolated growth hormone deficiency
- Pseudoachondroplasia
- Achondroplasia
- Hypochondroplasia
- Isolated growth hormone deficiency type III
- Laron syndrome
- FGFR3-related chondrodysplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
Parent facilities 0
Genetic Advices 0
Care facilities 2
Zentrum für Seltene Skeletterkrankungen im Kindes- und Jugendalter am Universitätsklinikum Köln
Centrum für Seltene Erkrankungen Köln (CESEK) Uniklinik Köln
Kerpener Straße 62
50937 Köln
- Fibrous dysplasia of bone
- Osteogenesis imperfecta
- Heart-hand syndrome
- Achondroplasia
- Omodysplasia
- Acromelic dysplasia
- Metachondromatosis
- Paralytic facial malformation
- Multiple osteochondromas
- Femur-fibula-ulna complex
- Rhizomelic chondrodysplasia punctata type 1
- Dysosteosclerosis
- OBSOLETE: Peripheral dysostosis
- Hypochondroplasia
- Brachydactyly-long thumb syndrome
Zentrum für Seltene Endokrine Erkrankungen (hormonelle Erkrankungen) am Universitätsklinikum Ulm
Universitätsklinikum Ulm Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm
Eythstraße 24
89075 Ulm
0731 50057401
0731 50057407
Website
Email
- Primary lipodystrophy
- Central diabetes insipidus
- Pseudohypoparathyroidism type 1A
- Rare diabetes mellitus
- Craniopharyngioma
- Multiple endocrine neoplasia
- Genetic obesity
- Congenital hypogonadotropic hypogonadism
- Addison disease
- Congenital isolated hyperinsulinism
- Prolactinoma
- Acquired lipodystrophy
- Acromegaly
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Spondyloepiphyseal dysplasia congenita
- Diastrophic dysplasia
- Silver-Russell syndrome
- Thanatophoric dysplasia
- Seckel syndrome
- Non-acquired isolated growth hormone deficiency
- Pseudoachondroplasia
- Achondroplasia
- Hypochondroplasia
- Isolated growth hormone deficiency type III
- Laron syndrome
- FGFR3-related chondrodysplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia