Syndromic craniosynostoses

Description

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.

Excludes

LD20.1 – Craniotelencephalic dysplasia
LD27.0Y – Sensenbrenner syndrome
LD28.0Y – Shprintzen-Goldberg craniosynostosis syndrome

Exclusions from above levels

http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Child codes

LD24.G0 – Pfeiffer syndrome
LD24.G1 – Crouzon disease
LD24.G2 – Apert syndrome
LD24.GY – Other specified syndromic craniosynostoses
LD24.GZ – Syndromic craniosynostoses, unspecified

Sibling codes

LD24.0 – Syndromes with micromelia
LD24.1 – Bone diseases with increased bone density
LD24.2 – Bone diseases with disorganised development of skeletal components
LD24.3 – Spondyloepiphyseal or spondyloepimetaphyseal dysplasias
LD24.4 – Spondylometaphyseal dysplasias
LD24.5 – Spondylodysplastic dysplasias
LD24.6 – Multiple epiphyseal dysplasia or pseudoachondroplasia
LD24.7 – Multiple metaphyseal dysplasias
LD24.8 – Acromelic dysplasias
LD24.9 – Acromesomelic dysplasias
LD24.A – Mesomelic or rhizomesomelic dysplasias
LD24.B – Short rib syndromes
LD24.C – Bent bone dysplasias
LD24.D – Slender bone dysplasias
LD24.E – Bone dysplasias with multiple joint dislocations
LD24.F – Progressive ossification of skin, skeletal muscle, fascia, tendons or ligaments
LD24.H – Dysostoses with predominant vertebral and costal involvement
LD24.J – Patellar dysostoses
LD24.K – Genetic bone diseases with decreased bone density
LD24.Y – Other specified syndromes with skeletal anomalies as a major feature
LD24.Z – Syndromes with skeletal anomalies as a major feature, unspecified

Foundation entity

Syndromic craniosynostoses – http://id.who.int/icd/entity/1908604930

Part of: LD24: Syndromes with skeletal anomalies as a major feature › 20: Developmental anomalies