Crouzon syndrome
MeSH: D003394ORPHA: 207
Overview
Congenital disorder of the skull and face
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Crouzon syndrome, sourced from HPO and Orphanet clinical annotations.
Narrow palateHydrocephalusBrachycephalyTurricephalyHypertelorismHypoplasia of the maxillaHigh foreheadHearing impairmentConductive hearing impairmentConvex nasal ridgeChoanal atresiaStrabismusPtosisConjunctivitisProptosisIris colobomaAmblyopiaOptic atrophyAbnormal skull morphologyAcanthosis nigricansMelanocytic nevusHypopigmented skin patchesCerebellar hypoplasiaAbnormal facial shapeFrontal bossingRespiratory insufficiencyChiari malformationHeadacheIncreased intracranial pressureAbnormal sacrum morphologyMultiple suture craniosynostosisNarrow internal auditory canalMidface retrusion
Classification & Codes
MeSH Code
D003394Orphanet Code
ORPHA:207Crouzon syndrome
| MeSH | D003394 |
| Orphanet | ORPHA:207 |
| Treatments | 0 drug(s) |
| Symptoms on record | 33 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO