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Maxillonasal dysplasia, Binder type MeSH Supplementary Concept Data 2022


MeSH Supplementary
Maxillonasal dysplasia, Binder type
Unique ID
C536036
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C536036
Entry Term(s)
Binder syndrome
Registry Number
0
Heading Mapped to
*Maxillofacial Abnormalities
Frequency
32
Note
Maxillofacial abnormalities characterized by a short nose with a flat bridge, a short columella, an acute nasolabial angle, perialar flatness, a convex upper lip, and a tendency to an ANGLE CLASS III MALOCCLUSION. Critical features of the syndrome appear to be midfacial hypoplasia, lack of anterior nasal spine, and malocclusion. May be hereditary (autosomal recessive) or multifactorial. OMIM: 155050
Date of Entry
2010/08/25
Revision Date
2015/08/18
Maxillonasal dysplasia, Binder type Preferred
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