Hallermann–Streiff syndrome
Rare congenital disorder / From Wikipedia, the free encyclopedia
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Hallermann–Streiff syndrome is a congenital disorder that affects growth, cranial development, hair-growth, and dental development. There are fewer than 200 people with the syndrome worldwide.[citation needed] One notable organization that is supporting people with Hallermann–Streiff syndrome is the Germany-based "Schattenkinder e.V".[1]
Quick Facts Other names, Specialty ...
Hallermann–Streiff syndrome | |
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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 |
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