Pfeiffer syndrome type 3 (Q94911): Difference between revisions
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A síndrome de Pfeiffer tipo 3 é um tipo grave frequente de síndrome de Pfeiffer e é caracterizada por craniossinostose bicoronal, graves distúrbios funcionais associados e anormalidades nas mãos, pés e cotovelos. | |||||||||||||||
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Pfeiffer syndrome type 3 is a frequent severe type of Pfeiffer syndrome and is characterised by bicoronal craniosynostosis, severe associated functional disorders, and hand, foot and elbow abnormalities. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1910513449 / rank | |||||||||||||||
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CID11:ID_1910513449 | |||||||||||||||
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dki-india-ID_1910513449 | |||||||||||||||
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| 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
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 10:27, 16 August 2026
Pfeiffer syndrome type 3 is a frequent severe type of Pfeiffer syndrome and is characterised by bicoronal craniosynostosis, severe associated functional disorders, and hand, foot and elbow abnormalities.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1910513449 |
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| English | Pfeiffer syndrome type 3 |
Pfeiffer syndrome type 3 is a frequent severe type of Pfeiffer syndrome and is characterised by bicoronal craniosynostosis, severe associated functional disorders, and hand, foot and elbow abnormalities. |
Statements
CID11:ID_1910513449
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dki-india-ID_1910513449
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Concluído
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15 August 2026
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