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Craniosynostosis

rare

Craniosynostosis is defined as the premature fusion of one or more cranial sutures leading to secondary distortion of skull shape resulting in skull deformities with a variable presentation. Craniosynostosis may occur in an isolated setting or as part of a syndrome.

Identifiers
MONDO:0015469 Orphanet:1531
Part of
Hereditary diseaseSynostosis
Also known as
craniosynostosis syndrome · CSO · premature closure of cranial sutures

Subtypes

All diseases Rare only
Disease Subtypes
Syndromic craniosynostosis 69
Craniosynostosis syndrome, autosomal recessive 11
Isolated craniosynostosis 8
Hordnes Engebretsen Knudtson syndrome
Iida Kannari syndrome
Craniosynostosis Fontaine type
Craniosynostosis Maroteaux Fonfria type
Craniosynostosis alopecia brain defect
Craniosynostosis arthrogryposis cleft palate
Craniosynostosis autosomal dominant
Craniosynostosis cleft lip palate arthrogryposis
Craniosynostosis contractures cleft
Craniosynostosis exostoses nevus epibulbar dermoid
Craniosynostosis intellectual disability heart defects
Craniosynostosis with ectopia lentis
Craniosynostosis with ocular abnormalities and hallucal defects
Craniosynostosis, Adelaide type
Mehta lewis patton syndrome
Non-syndromic bicoronal and metopic craniosynostosis
Non-syndromic bicoronal and sagittal craniosynostosis
Non-syndromic bilambdoid craniosynostosis
Non-syndromic metopic and sagittal craniosynostosis
Non-syndromic multisutural craniosynostosis
Non-syndromic non-specific multisutural craniosynostosis
Non-syndromic unicoronal and sagittal craniosynostosis
Non-syndromic unicoronal craniosynostosis
Non-syndromic unifrontosphenoidal craniosynostosis
Non-syndromic unilambdoid craniosynostosis
Non-syndromic unisquamosal craniosynostosis

Rare disease

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