Hallermann–Streiff syndrome
| Hallermann–Streiff syndrome | |
|---|---|
| Other names | Oculomandibulofacial syndrome, François dyscephalic syndrome, Hallermann–Streiff–François syndrome, oculomandibulodyscephaly with hypotrichosis, Aubry syndrome, Ullrich–Fremery-Dohna syndrome |
| Girl with Hallermann-Streiff syndrome displaying characteristic facial features | |
| Specialty | Medical genetics |
Hallermann–Streiff syndrome is a congenital disorder that affects the eyes, general growth, cranial development, hair-growth, and dental development. There are fewer than 200 people with the syndrome worldwide. One notable organization that is supporting people with Hallermann–Streiff syndrome is the Germany-based "Schattenkinder e.V".[1]
- ^ "Herzlich willkommen!". schattenkinder.info. Retrieved 2020-05-07.