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