IVIC Syndrome
MeSH: C535544ORPHA: 2307
Overview
IVIC syndrome is a very rare genetic malformation syndrome characterized by upper limb anomalies (radial ray defects, carpal bone fusion), extraocular motor disturbances, and congenital bilateral non-progressive mixed hearing loss
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 IVIC Syndrome, sourced from HPO and Orphanet clinical annotations.
Hearing impairmentStrabismusJoint stiffnessHypoplasia of the radiusSevere short statureTriphalangeal thumbScoliosisRadioulnar synostosisSynostosis of carpal bonesAbnormal dermatoglyphicsShort thumbRectovaginal fistulaPreaxial hand polydactylyThrombocytopeniaIncreased total leukocyte countAnal atresiaAplastic clavicleArrhythmia
Classification & Codes
MeSH Code
C535544Orphanet Code
ORPHA:2307IVIC Syndrome
| MeSH | C535544 |
| Orphanet | ORPHA:2307 |
| Treatments | 0 drug(s) |
| Symptoms on record | 18 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO