Phocomelia, Schinzel type (Q94205): Difference between revisions
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A síndrome de focomelia Schinzel, também chamada de síndrome de hipoplasia/aplasia de membros/pelve, é caracterizada por malformações esqueléticas, incluindo deficiências de membros intercalares (focomelia às vezes combinada com polidactilia, oligodactilia ou ectrodactilia), ossos pélvicos ausentes ou hipoplásicos (incluindo agenesia ou hipoplasia sacral), defeitos cranianos (frequentemente um defeito do osso occipital com ou sem meningocele). | |||||||||||||||
| description / en | description / en | ||||||||||||||
Schinzel phocomelia syndrome, also called limb/pelvis hypoplasia/aplasia syndrome, is characterised by skeletal malformations including intercalary limb deficiencies (phocomelia sometimes combined with polydactyly, oligodactyly or ectrodactyly), absent or hypoplastic pelvic bones (including sacral agenesis or hypoplasia), skull defects (frequently a defect of the occipital bone with or without meningocele). | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1732271544 / rank | |||||||||||||||
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CID11:ID_1732271544 | |||||||||||||||
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dki-india-ID_1732271544 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 09:20, 16 August 2026
Schinzel phocomelia syndrome, also called limb/pelvis hypoplasia/aplasia syndrome, is characterised by skeletal malformations including intercalary limb deficiencies (phocomelia sometimes combined with polydactyly, oligodactyly or ectrodactyly), absent or hypoplastic pelvic bones (including sacral agenesis or hypoplasia), skull defects (frequently a defect of the occipital bone with or without meningocele).
| Language | Label | Description | Also known as |
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| default for all languages | ID_1732271544 |
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| English | Phocomelia, Schinzel type |
Schinzel phocomelia syndrome, also called limb/pelvis hypoplasia/aplasia syndrome, is characterised by skeletal malformations including intercalary limb deficiencies (phocomelia sometimes combined with polydactyly, oligodactyly or ectrodactyly), absent or hypoplastic pelvic bones (including sacral agenesis or hypoplasia), skull defects (frequently a defect of the occipital bone with or without meningocele). |
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CID11:ID_1732271544
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dki-india-ID_1732271544
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Concluído
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15 August 2026
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