Microcephalic primordial dwarfism, Montreal type
All Entries 2
Zentrum für seltene Entwicklungsstörungen am kbo-Kinderzentrum München
Klinikum rechts der Isar der Technischen Universität München Zentrum für Seltene Erkrankungen am Klinikum rechts der Isar der Technischen Universität München
Heiglhofstr. 65
81377 München
089 710090
089 71009253
Website
Email
- Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
- Rubinstein-Taybi syndrome
- Infantile spasms syndrome
- Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
- Hennekam syndrome
- Achondroplasia
- Aicardi-Goutières syndrome
- ADNP syndrome
- GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
- 22q11.2 deletion syndrome
- KBG syndrome
- Kabuki syndrome
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Non-acquired isolated growth hormone deficiency
- Achondroplasia
- Silver-Russell syndrome
- Pseudoachondroplasia
- Laron syndrome
- Seckel syndrome
- Hypochondroplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- FGFR3-related chondrodysplasia
- Thanatophoric dysplasia
- Spondyloepiphyseal dysplasia congenita
- Diastrophic dysplasia
- Isolated growth hormone deficiency type III
Parent facilities 0
Genetic Advices 0
Care facilities 1
Zentrum für seltene Entwicklungsstörungen am kbo-Kinderzentrum München
Klinikum rechts der Isar der Technischen Universität München Zentrum für Seltene Erkrankungen am Klinikum rechts der Isar der Technischen Universität München
Heiglhofstr. 65
81377 München
089 710090
089 71009253
Website
Email
- Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
- Rubinstein-Taybi syndrome
- Infantile spasms syndrome
- Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
- Hennekam syndrome
- Achondroplasia
- Aicardi-Goutières syndrome
- ADNP syndrome
- GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
- 22q11.2 deletion syndrome
- KBG syndrome
- Kabuki syndrome
Supportgroups 1
Bundesverband Kleinwüchsige Menschen und ihre Familien (BKMF) e.V.
Leinestraße 2
28199
Bremen
- Non-acquired isolated growth hormone deficiency
- Achondroplasia
- Silver-Russell syndrome
- Pseudoachondroplasia
- Laron syndrome
- Seckel syndrome
- Hypochondroplasia
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- FGFR3-related chondrodysplasia
- Thanatophoric dysplasia
- Spondyloepiphyseal dysplasia congenita
- Diastrophic dysplasia
- Isolated growth hormone deficiency type III