Wiedemann-Rautenstrauch syndrome
ICD-10: E34.8MeSH: C536423ORPHA: 2500
Overview
very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism
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 Wiedemann-Rautenstrauch syndrome, sourced from HPO and Orphanet clinical annotations.
Joint hypermobilityAbnormality of the skinThin skinFine hairShort statureIrregular hyperpigmentationPrematurely aged appearanceAplasia/Hypoplasia of the skinLipoatrophyMicrognathiaConvex nasal ridgeIntellectual disabilityShort footScoliosisExcessive wrinkled skinTelangiectasia of the skinSmall handSkeletal dysplasiaSkin ulcer
Classification & Codes
ICD-10 Code
E34.8MeSH Code
C536423Orphanet Code
ORPHA:2500Wiedemann-Rautenstrauch syndrome
| ICD-10 | E34.8 |
| MeSH | C536423 |
| Orphanet | ORPHA:2500 |
| Treatments | 0 drug(s) |
| Symptoms on record | 19 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO