Syndromic craniosynostoses (Q46571): Difference between revisions
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Qualquer síndrome causada por fusão prematura de seções do crânio infantil. Essas síndromes são caracterizadas por crescimento compensatório desfigurante do crânio. Essas síndromes também podem se manifestar com piora frequente da cefaleia matinal, vômitos recorrentes, desproporção cefalocraniana, pressão intracraniana aumentada, atrofia óptica, cegueira ou atraso no desenvolvimento. | |||
| description / en | description / en | ||
Any syndrome caused by premature fusing of sections of the infant skull. These syndromes are characterised by disfiguring compensatory growth of the skull. These syndromes may also present with frequent worsening morning headache, recurrent vomiting, cephalocranial disproportion, raised intracranial pressure, optic atrophy, blindness, or developmental delay. | |||
Revision as of 15:14, 13 August 2026
Any syndrome caused by premature fusing of sections of the infant skull. These syndromes are characterised by disfiguring compensatory growth of the skull. These syndromes may also present with frequent worsening morning headache, recurrent vomiting, cephalocranial disproportion, raised intracranial pressure, optic atrophy, blindness, or developmental delay.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD24.G |
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| English | Syndromic craniosynostoses |
Any syndrome caused by premature fusing of sections of the infant skull. These syndromes are characterised by disfiguring compensatory growth of the skull. These syndromes may also present with frequent worsening morning headache, recurrent vomiting, cephalocranial disproportion, raised intracranial pressure, optic atrophy, blindness, or developmental delay. |
