Laurin-Sandrow syndrome
MeSH: C535689ORPHA: 2378
Overview
developmental defect during embryogenesis
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 Laurin-Sandrow syndrome, sourced from HPO and Orphanet clinical annotations.
Preaxial hand polydactylyTriphalangeal thumbToe syndactylyPreaxial foot polydactylyAbnormal metacarpal morphologyFinger syndactylyTarsal synostosisAplasia/Hypoplasia of the thumbMirror image polydactylyAbnormality of the noseUnderdeveloped nasal alaeProminent noseDepressed nasal ridgeLimitation of joint mobilityTalipesShort columellaAbnormality of the wristAbsent radiusAbsent tibiaFibular duplicationLimb duplicationCryptorchidismHydrocephalusHypertelorismIntellectual disabilityHypotoniaDownturned corners of mouthAplasia/Hypoplasia of the corpus callosum
Classification & Codes
MeSH Code
C535689Orphanet Code
ORPHA:2378Laurin-Sandrow syndrome
| MeSH | C535689 |
| Orphanet | ORPHA:2378 |
| Treatments | 0 drug(s) |
| Symptoms on record | 28 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO