Pfeiffer syndrome type 1 (Q94917): Difference between revisions
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A síndrome de Pfeiffer tipo 1 é um tipo raro de síndrome de Pfeiffer com gravidade leve a moderada e é caracterizada por craniossinostose bicoronal, malformações variáveis nos dedos das mãos e dos pés e, geralmente, desenvolvimento intelectual normal. | |||
| description / en | description / en | ||
Pfeiffer syndrome type 1 is an infrequent type of Pfeiffer syndrome with mild to moderate severity and is characterised by bicoronal craniosynostosis, variable finger and toe malformations, and usually normal intellectual development. | |||
Revision as of 10:28, 16 August 2026
Pfeiffer syndrome type 1 is an infrequent type of Pfeiffer syndrome with mild to moderate severity and is characterised by bicoronal craniosynostosis, variable finger and toe malformations, and usually normal intellectual development.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_490354109 |
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| English | Pfeiffer syndrome type 1 |
Pfeiffer syndrome type 1 is an infrequent type of Pfeiffer syndrome with mild to moderate severity and is characterised by bicoronal craniosynostosis, variable finger and toe malformations, and usually normal intellectual development. |
