Diseases

Craniofacial Dysostosis

Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia.

MeSH Record

Classification

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MeSH Record

See Also

MeSH Record

Synonyms

17 entry terms
  • Craniofacial Dysarthrosis
  • Craniofacial Dysostosis Syndrome
  • Dysostosis, Craniofacial
  • Craniofacial Dysarthroses
  • Craniofacial Dysostoses
  • Craniofacial Dysostosis Syndromes
  • Dysarthroses, Craniofacial
  • Dysarthrosis, Craniofacial
  • Dysostoses, Craniofacial
  • Craniofacial Dysostosis Type 1
  • Craniofacial Dysostosis, Type I
  • Crouzon Craniofacial Dysostosis
  • Crouzon Disease
  • Crouzon Syndrome
  • Crouzon's Disease
  • Craniofacial Dysostosis, Crouzon
  • Crouzons Disease

MeSH Record

Aspects Covered

34 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

Indexing Annotation

"craniofacial dysmorphism" does not go here: index under FACIAL BONES / abnorm + SKULL / abnorm but not also ABNORMALITIES, MULTIPLE

MeSH Hierarchy

Tree Numbers

MeSH Record

NLM Classification

WE 705

AMA Style

References

  1. National Library of Medicine. Craniofacial Dysostosis. Medical Subject Headings (MeSH). 2026. Unique ID D003394. http://id.nlm.nih.gov/mesh/2026/D003394
  2. Craniofacial Dysostosis. In: Wikipedia. https://en.wikipedia.org/wiki/Crouzon_syndrome
  3. Craniofacial Dysostosis. In: Wikidata. https://www.wikidata.org/wiki/Q779250