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).
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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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Property / Canonical URI: https://id.who.int/icd/entity/1665391511 / rank
 
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CID11:ID_1665391511
Property / CURIE: CID11:ID_1665391511 / rank
 
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dki-india-ID_1665391511
Property / Canary Token: dki-india-ID_1665391511 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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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).
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ID_1665391511
    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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