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DiseaseQ2291593· pop 14· linked from 109 articles

scaphocephaly

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Also known as Scaphycephaly, Sagittal Synostosis

Scaphocephaly or sagittal craniosynostosis is a type of cephalic disorder which occurs when there is a premature fusion of the sagittal suture. Premature closure results in limited lateral expansion of the skull, resulting in a characteristic long, narrow head. The skull base is typically spared. The word comes .

Key facts

Medical condition (new).name
Scaphocephaly
Medical condition (new).image
Scaphocephalic cranium.jpg
Medical condition (new).caption
Boy with Scaphocephaly
Medical condition (new).pronounce
skaf-o-SEF-aly
Medical condition (new).alt
Boy with Scaphocephaly

via Wikipedia infobox

Health references

ICD-10
Q75.001 — Craniosynostosis, unspecified type, unilateral
Source: U.S. National Library of Medicine (ICD-10-CM · MedlinePlus). Not medical advice.

Clinical Trials

6 registered

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Encyclopedic overview

9 sections
Contents
  • Etiology
  • Diagnosis and evaluation
  • Classification
  • Treatment
  • Terminology
  • See also
  • References
  • External links
  • References

Scaphocephaly or sagittal craniosynostosis is a type of cephalic disorder which occurs when there is a premature fusion of the sagittal suture. Premature closure results in limited lateral expansion of the skull, resulting in a characteristic long, narrow head. The skull base is typically spared. The word comes .

Scaphocephaly is the most common of the craniosynostosis conditions and accounts for approximately 50% of all craniosynostosis. It is most commonly idiopathic (non-syndromic).

Excerpted from Wikipedia’s “scaphocephaly” article, available under the CC BY-SA 4.0 licence.