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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