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craniosynostosis
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craniosynostosis

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Also known as craniostenosis, premature closure of cranial sutures, craniosynostosis syndrome

Craniosynostosis is a condition in which one or more of the fibrous sutures in a young infant's skull prematurely fuses by turning into bone (ossification), thereby changing the growth pattern of the skull. Because the skull cannot expand perpendicular to the fused suture, it compensates by growing more in the direction parallel to the closed sutures. Sometimes the resulting growth pattern provides the necessary space for the growing brain, but results in an abnormal head shape and abnormal facial features. In cases in which the compensation does not effectively provide enough space for the gr

Key facts

Medical condition.name
Craniosynostosis
Medical condition.synonyms
Craniostenosis
Medical condition.image
Cranialsynostosis.jpg
Medical condition.caption
Child with premature closure (craniosynostosis) of the lambdoid suture. Notice the swelling on the right side of the head
Medical condition.specialty
Medical genetics
Medical condition.complications
Increased intracranial pressure
Medical condition.onset
during young age

via Wikipedia infobox

Research

10,134 papers

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Wikidata facts

Image
Cranialsynostosis.jpg
Show 5 more facts
NCI Thesaurus ID
C84655
prevalence
0.000045
Commons category
Craniosynostosis
ICPC 2 ID
L82
Sources (4)

via Wikidata · CC0

~38 min read

Article

42 sections
Contents
  • Signs and symptoms
  • Scaphocephaly
  • Trigonocephaly
  • Plagiocephaly
  • Anterior plagiocephaly
  • Posterior plagiocephaly
  • Brachycephaly
  • Turricephaly
  • Pansynostosis
  • Other forms
  • Complications
  • Elevated intracranial pressure
  • Obstructive sleep apnea
  • Abnormalities in the skull base
  • Neurobehavioural impairment
  • Causes
  • Biomechanical factors
  • Environmental factors
  • Hormonal factors
  • Genetic factors
  • Cranial sutures
  • Diagnosis
  • Elevated ICP
  • Physical examination
  • Medical imaging
  • Classification
  • Differential diagnosis
  • Deformational plagiocephaly
  • Primary microcephaly
  • Treatment
  • Timing of surgery
  • Specific sutures
  • Sagittal craniosynostosis/scaphocephaly
  • Metopic synostosis/trigonocephaly
  • Unilateral coronal synostosis/anterior plagiocephaly
  • Unilateral lambdoid synostosis/posterior plagiocephaly
  • Bilateral coronal synostosis/brachycephaly
  • Pansynostosis/kleeblattschädel
  • Complications
  • Epidemiology
  • References
  • External links

Craniosynostosis is a condition in which one or more of the fibrous sutures in a young infant's skull prematurely fuses by turning into bone (ossification), thereby changing the growth pattern of the skull. Because the skull cannot expand perpendicular to the fused suture, it compensates by growing more in the direction parallel to the closed sutures. Sometimes the resulting growth pattern provides the necessary space for the growing brain, but results in an abnormal head shape and abnormal facial features. In cases in which the compensation does not effectively provide enough space for the growing brain, craniosynostosis results in increased intracranial pressure leading possibly to visual impairment, sleeping impairment, eating difficulties, or an impairment of mental development combined with a significant reduction in IQ.

Craniosynostosis occurs in one in 2000 births. Craniosynostosis is part of a syndrome in 15% to 40% of affected patients, but it usually occurs as an isolated condition. The term is from cranio, cranium; + syn, together; + ost, relating to bone; + osis, denoting a condition. Craniosynostosis is the opposite of metopism.

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