LD25.3 Craniofacial dysostoses
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Syndromes caused by abnormal development of skull and facial bones. They may present with acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, or hypoplastic maxilla. Non-syndromic craniosynostosis, which is predominantly sporadic, is coded elsewhere.
exclusions
- Acrofacial dysostosis, Nager type (LD25.2)
- Postaxial acrofacial dysostosis (LD25.2)
- Acrofacial dysostosis, Weyers type (LD25.2)
- Frontometaphyseal dysplasia (LD25.1)
- Craniosynostosis (LB70.0)
synonyms
- Craniofacial dysostoses
- Craniofacial dysostosis
- Oculomaxillofacial dysostosis
- Frontofacionasal dysostosis
- Frontonasal dysplasia
- Acromelic frontonasal dysplasia
- Toriello syndrome
- Acrofrontofacionasal dysostosis
- Richieri-Costa-Colletto syndrome
- Familial osteodysplasia, Anderson type
- Craniofrontonasal dysplasia
- Gollop syndrome
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