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
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Email
- Autosomal dominant polycystic kidney disease
- Osteogenesis imperfecta
- Large congenital melanocytic nevus
- 22q11.2 deletion syndrome
- Neurocutaneous melanocytosis
- Digestive tract malformation
- Autosomal recessive polycystic kidney disease
- Neural tube defect
- Rare bone disease
- Diaphragmatic or abdominal wall malformation
Zentrum für seltene kranio-orofaziale Erkrankungen am Universitätsklinikum Heidelberg
Centre for Rare Diseases Heidelberg Universitätsklinikum Heidelberg
Im Neuenheimer Feld 400
69120 Heidelberg
- Non-syndromic metopic craniosynostosis
- Seckel syndrome
- Van der Woude syndrome
- Orofaciodigital syndrome type 2
- Papillon-Lefèvre syndrome
- Saethre-Chotzen syndrome
- Crouzon syndrome
- Paramedian facial cleft
- Oblique facial cleft
- Facial cleft
- GAPO syndrome
- Noonan syndrome
- Apert syndrome
- Median facial cleft
- Isolated Pierre Robin syndrome