Angioosteohypotrophic syndrome
Parent facilities 0
Genetic Advices 1
Institut für Medizinische Genetik und Humangenetik an der Charité Berlin
Berliner Centrum für Seltene Erkrankungen (BCSE) Charité Universitätsmedizin Berlin
Augustenburger Platz 1
13353 Berlin
030 450569122
030 450569915
Website
Care facilities 2
Altonaer Kinderkrankenhaus
Bleickenallee 38
22763 Hamburg
040 889080
040 88908366
Website
Email
- Autosomal dominant polycystic kidney disease
- Osteogenesis imperfecta
- Diaphragmatic or abdominal wall malformation
- Large congenital melanocytic nevus
- Digestive tract malformation
- Neural tube defect
- Autosomal recessive polycystic kidney disease
- Rare bone disease
- 22q11.2 deletion syndrome
- Neurocutaneous melanocytosis
Zentrum für seltene kranio-orofaziale Erkrankungen am Universitätsklinikum Heidelberg
Universitätsklinikum Heidelberg Centre for Rare Diseases Heidelberg
Im Neuenheimer Feld 400
69120 Heidelberg
- Saethre-Chotzen syndrome
- Apert syndrome
- Van der Woude syndrome
- Oblique facial cleft
- Isolated Pierre Robin syndrome
- Non-syndromic metopic craniosynostosis
- Median facial cleft
- Seckel syndrome
- Noonan syndrome
- GAPO syndrome
- Papillon-Lefèvre syndrome
- Orofaciodigital syndrome type 2
- Facial cleft
- Paramedian facial cleft
- Crouzon syndrome