Oromandibular-limb hypogenesis syndrome (Q94829): Difference between revisions
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15 August 2026
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Latest 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). |
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CID11:ID_1665391511
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dki-india-ID_1665391511
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Concluído
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15 August 2026
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