Adams-Oliver syndrome
MeSH: C538225ORPHA: 974
Overview
syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs
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 Adams-Oliver syndrome, sourced from HPO and Orphanet clinical annotations.
Cutis marmorataAplasia cutis congenitaCalvarial skull defectFailure to thriveAbnormality of the lower limbAbnormality of the upper limbAbsent handAplasia/Hypoplasia of the skinSparse hairAbsent toeHydrocephalusStrabismusCataractMicrophthalmiaBrachydactylySplit handTetralogy of FallotAbnormal pulmonary valve morphologyTalipesPulmonary artery atresiaAbnormal metacarpal morphologyFinger syndactylyShort distal phalanx of fingerIntellectual disabilitySeizureHemiparesisHypertoniaCirrhosisPortal hypertensionAscitesAlopeciaPremature birthHypoplastic fingernailAbsent fingernailThrombocytopeniaDecreased total leukocyte countEsophageal varixEncephalocelePulmonary arterial hypertensionPorencephalic cystGastrointestinal hemorrhageEEG abnormalityCongenital hepatic fibrosisPeriventricular leukomalaciaAplastic/hypoplastic toenailArteriovenous malformation
Classification & Codes
MeSH Code
C538225Orphanet Code
ORPHA:974Adams-Oliver syndrome
| MeSH | C538225 |
| Orphanet | ORPHA:974 |
| Treatments | 0 drug(s) |
| Symptoms on record | 46 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO