Carpenter syndrome
MeSH: C563187ORPHA: 65759
Overview
acrocephalosyndactylia characterized by craniosynostosis, acrocephaly, obesity, syndactyly and polydactyly
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 Carpenter syndrome, sourced from HPO and Orphanet clinical annotations.
BrachydactylyToe syndactylyFinger syndactylyCryptorchidismTall statureMacrocephalyOxycephalyNarrow faceEpicanthusHypertelorismAbnormal skull morphologySyndactylyIntellectual disabilityPlagiocephalyCraniosynostosisObesityExternal genital hypoplasiaClinodactyly of the 5th fingerShort palmProminent metopic ridgePolydactylyTurricephalyWide noseDepressed nasal ridgeAbnormal cornea morphologyStrabismusPostaxial hand polydactylyPreaxial foot polydactylyCloverleaf skullGenu valgumBroad thumbAbnormal reproductive system morphologyAbnormal cardiovascular system morphologyUmbilical herniaPatent ductus arteriosusPolyspleniaTalipes equinovarusKyphoscoliosisShort 4th metacarpalCamptodactyly of finger
Classification & Codes
MeSH Code
C563187Orphanet Code
ORPHA:65759Carpenter syndrome
| MeSH | C563187 |
| Orphanet | ORPHA:65759 |
| Treatments | 0 drug(s) |
| Symptoms on record | 40 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO