CIM11 LD24.G
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Syndromic craniosynostoses
- chapitre
- 20 Developmental anomalies
- bloc
- Multiple developmental anomalies or syndromes
- definition
- 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
- exclusions
- Sensenbrenner syndrome | Shprintzen-Goldberg craniosynostosis syndrome | Craniotelencephalic dysplasia
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1908604930 ↗