Maxillonasal dysplasia (Q53963): Difference between revisions
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Síndrome de Binder é uma anomalia de desenvolvimento rara, que afeta primariamente a parte anterior da maxila e o complexo nasal. Os indivíduos afetados tipicamente apresentam uma face média anormalmente plana e subdesenvolvida (hipoplasia facial média), com um nariz anormalmente curto e ponte nasal plana, maxila subdesenvolvida, mandíbula relativamente protuberante e/ou uma "sobremordida reversa" (ou má oclusão de classe III). | |||
| description / en | description / en | ||
Binder syndrome is a rare developmental anomaly, affecting primarily the anterior part of the maxilla and nasal complex. Affected individuals typically have an unusually flat, underdeveloped midface (midfacial hypoplasia), with an abnormally short nose and flat nasal bridge, underdeveloped upper jaw, relatively protruding lower jaw and/or a 'reverse overbite'' (or class III malocclusion). | |||
Revision as of 01:34, 14 August 2026
Binder syndrome is a rare developmental anomaly, affecting primarily the anterior part of the maxilla and nasal complex. Affected individuals typically have an unusually flat, underdeveloped midface (midfacial hypoplasia), with an abnormally short nose and flat nasal bridge, underdeveloped upper jaw, relatively protruding lower jaw and/or a 'reverse overbite'' (or class III malocclusion).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1099755052 |
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| English | Maxillonasal dysplasia |
Binder syndrome is a rare developmental anomaly, affecting primarily the anterior part of the maxilla and nasal complex. Affected individuals typically have an unusually flat, underdeveloped midface (midfacial hypoplasia), with an abnormally short nose and flat nasal bridge, underdeveloped upper jaw, relatively protruding lower jaw and/or a 'reverse overbite'' (or class III malocclusion). |
