Bazex–Dupré–Christol syndrome
MeSH: C537663ORPHA: 113
Overview
Bazex-DuprC)-Christol syndrome is a rare genodermatosis with a predisposition to early-onset basal cell carcinomas
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 Bazex–Dupré–Christol syndrome, sourced from HPO and Orphanet clinical annotations.
Coarse hairMiliaSubcutaneous noduleSparse scalp hairBasal cell carcinomaPili tortiSparse hairTrichorrhexis nodosaSparse eyebrowSparse or absent eyelashesMacrotiaAbnormal clavicle morphologyAbnormal finger morphologyHypoplasia of the ear cartilageExostoses
Classification & Codes
MeSH Code
C537663Orphanet Code
ORPHA:113Bazex–Dupré–Christol syndrome
| MeSH | C537663 |
| Orphanet | ORPHA:113 |
| Treatments | 0 drug(s) |
| Symptoms on record | 15 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO