Glossopalatine ankylosis (Q105878): Difference between revisions
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Anquilose glossopalatina é uma doença pertencente ao grupo das síndromes oromandibular-hipogênese dos membros (OLHS) e é caracterizada pela presença de uma banda intraoral de espessura variável fixando a língua ao palato duro ou rebordo alveolar maxilar. Anomalias associadas incluem fenda palatina (caso em que a língua pode estar ligada ao septo nasal), hipoplasia mandibular, hipoplasia do lábio superior, hipodontia e anomalias variáveis nos membros (oligodactilia, sindactilia e polidactilia (ver estes termos), bem como malformações mais grave de membros). | |||
| description / en | description / en | ||
Glossopalatine ankylosis is a disorder belonging to the group of oromandibular-limb hypogenesis syndromes (OLHS) and is characterised by the presence of an intraoral band of variable thickness attaching the tongue to the hard palate or maxillary alveolar ridge. Associated anomalies include cleft palate (in which case the tongue may be attached to the nasal septum), mandibular hypoplasia, upper-lip hypoplasia, hypodontia and variable limb anomalies (oligodactyly, syndactyly and polydactyly (see these terms), as well as more severe limb malformations). | |||
Revision as of 12:27, 17 August 2026
Glossopalatine ankylosis is a disorder belonging to the group of oromandibular-limb hypogenesis syndromes (OLHS) and is characterised by the presence of an intraoral band of variable thickness attaching the tongue to the hard palate or maxillary alveolar ridge. Associated anomalies include cleft palate (in which case the tongue may be attached to the nasal septum), mandibular hypoplasia, upper-lip hypoplasia, hypodontia and variable limb anomalies (oligodactyly, syndactyly and polydactyly (see these terms), as well as more severe limb malformations).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1608847387 |
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| English | Glossopalatine ankylosis |
Glossopalatine ankylosis is a disorder belonging to the group of oromandibular-limb hypogenesis syndromes (OLHS) and is characterised by the presence of an intraoral band of variable thickness attaching the tongue to the hard palate or maxillary alveolar ridge. Associated anomalies include cleft palate (in which case the tongue may be attached to the nasal septum), mandibular hypoplasia, upper-lip hypoplasia, hypodontia and variable limb anomalies (oligodactyly, syndactyly and polydactyly (see these terms), as well as more severe limb malformations). |
