Binder syndrome
From WikiLectures
Synonyms: dysosteosis maxillonasalis, dysplasia maxillonasalis.
Named after the Austrian dentist Kurt Binder.
- Genetics
- OMIM: 155050
- The etiology is probably heterogeneous, if the syndrome repeats in families, then it shows autosomal dominant inheritance.[1]
- Characteristics
- flat short nose,
- crescent shaped nostrils,
- the base of the upper jaw is flat,
- pseudoprogeny,
- hypoplasia to aplasia of the sinus frontalis and the anterior nasal process of the jaw.
Links[edit | edit source]
Reference[edit | edit source]
- ↑ OMIM : Binders syndrome - Clinical synopsis [database]. Johns Hopkins University. [cit. 2011-04-24]. <http://omim.org/entry/155050>.
References[edit | edit source]
- LAZOVSKIS, Ilmars – DOBIÁŠ, Václav. Overview of clinical symptoms and syndromes. 2. edition. Avicenum, zdravotnické nakladatelství, 1990. 0 pp. ISBN 80-201-0043-1.
