Oromandibular-limb hypogenesis syndrome (Q94829): Difference between revisions
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Síndromes oromandibular-hipogênese dos membros são um grupo de complexos dismórficos (incluindo a síndrome de Charlie M, a síndrome de Hanhart e a anquilose glossopalatina) caracterizadas pela associação de graves defeitos assimétricos nos membros (envolvendo primariamente segmentos distais) e anormalidades da cavidade oral e mandíbula (hipoglossia, aglossia , micrognatia, anquilose glossopalatina, fenda palatina e anomalias gengivais). | |||
| description / en | description / en | ||
Oromandibular-limb hypogenesis syndromes are a group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) characterised by the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). | |||
Revision as of 10:20, 16 August 2026
Oromandibular-limb hypogenesis syndromes are a group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) characterised by the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1665391511 |
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| English | Oromandibular-limb hypogenesis syndrome |
Oromandibular-limb hypogenesis syndromes are a group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) characterised by the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). |
