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
- Brachydactyly-long thumb syndrome
- Omodysplasia
- OBSOLETE: Peripheral dysostosis
- Rhizomelic chondrodysplasia punctata type 1
- Multiple osteochondromas
- Acromelic dysplasia
- Metachondromatosis
- Paralytic facial malformation
- Osteogenesis imperfecta
- Achondroplasia
- Heart-hand syndrome
- Hypochondroplasia
- Femur-fibula-ulna complex
- Fibrous dysplasia of bone
- Dysosteosclerosis
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
- Addison disease
- Prolactinoma
- Congenital isolated hyperinsulinism
- Central diabetes insipidus
- Multiple endocrine neoplasia
- Congenital hypogonadotropic hypogonadism
- Rare diabetes mellitus
- Pseudohypoparathyroidism type 1A
- Genetic obesity
- Acquired lipodystrophy
- Acromegaly
- Craniopharyngioma
- Primary lipodystrophy
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Achondroplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Non-acquired isolated growth hormone deficiency
- Hypochondroplasia
- Isolated growth hormone deficiency type III
- Spondyloepiphyseal dysplasia congenita
- Thanatophoric dysplasia
- Silver-Russell syndrome
- Diastrophic dysplasia
- Pseudoachondroplasia
- FGFR3-related chondrodysplasia
- Laron syndrome
- Seckel syndrome
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
- Brachydactyly-long thumb syndrome
- Omodysplasia
- OBSOLETE: Peripheral dysostosis
- Rhizomelic chondrodysplasia punctata type 1
- Multiple osteochondromas
- Acromelic dysplasia
- Metachondromatosis
- Paralytic facial malformation
- Osteogenesis imperfecta
- Achondroplasia
- Heart-hand syndrome
- Hypochondroplasia
- Femur-fibula-ulna complex
- Fibrous dysplasia of bone
- Dysosteosclerosis
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
- Addison disease
- Prolactinoma
- Congenital isolated hyperinsulinism
- Central diabetes insipidus
- Multiple endocrine neoplasia
- Congenital hypogonadotropic hypogonadism
- Rare diabetes mellitus
- Pseudohypoparathyroidism type 1A
- Genetic obesity
- Acquired lipodystrophy
- Acromegaly
- Craniopharyngioma
- Primary lipodystrophy
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Achondroplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Non-acquired isolated growth hormone deficiency
- Hypochondroplasia
- Isolated growth hormone deficiency type III
- Spondyloepiphyseal dysplasia congenita
- Thanatophoric dysplasia
- Silver-Russell syndrome
- Diastrophic dysplasia
- Pseudoachondroplasia
- FGFR3-related chondrodysplasia
- Laron syndrome
- Seckel syndrome