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. | |||
| description / en | description / en | ||
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. | |||
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 |
|---|---|---|---|
| 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. |
