Mietens syndrome
MeSH: C537444ORPHA: 2557
Overview
Mietens syndrome is a very rare syndrome consisting of corneal opacity, nystagmus, strabismus, flexion contracture of the elbows with dislocation of the head of the radius and abnormally short ulnae and radii
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 Mietens syndrome, sourced from HPO and Orphanet clinical annotations.
StrabismusNystagmusIntellectual disabilityGlobal developmental delaySpecific learning disabilityJoint stiffnessMutismAphasiaHypoplasia of the radiusHypoplasia of the ulnaElbow dislocationShort noseSevere short statureCorneal opacityEcholaliaHigh foreheadWide nasal bridgeWide noseElbow ankylosisClinodactyly of the 5th fingerMicrocephalyMicrocorneaCataractSclerocorneaHip dysplasiaMetatarsus adductusTalipesCoxa valgaCoxa varaHip dislocationAbnormal fibula morphologyAvascular necrosis of the capital femoral epiphysis
Classification & Codes
MeSH Code
C537444Orphanet Code
ORPHA:2557Mietens syndrome
| MeSH | C537444 |
| Orphanet | ORPHA:2557 |
| Treatments | 0 drug(s) |
| Symptoms on record | 32 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO