Syndromic craniosynostoses

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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.

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ICD-11 MMS

20 Developmental anomalies

Multiple developmental anomalies or syndromes (LD20-LD2Z)

LD24 Syndromes with skeletal anomalies as a major feature

Syndromic craniosynostoses

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

exclusions

code elsewhere

sections/codes in this section (LD24.G-LD24.G)