acral dystrophic epidermolysis bullosa
ORPHA: 158673
Overview
Acral dystrophic epidermolysis bullosa is a very rare subtype of dystrophic epidermolysis bullosa (DEB, see this term) characterized by blistering confined primarily to the hands and feet
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 acral dystrophic epidermolysis bullosa, sourced from HPO and Orphanet clinical annotations.
Thin skinPalmoplantar hyperkeratosisCutaneous photosensitivityTelangiectasiaPoikilodermaFragile skinMiliaDystrophic toenailEsophageal strictureAbnormality of the lower limbDermal atrophyCrusting erythematous dermatitisAbnormal blistering of the skinDystrophic fingernailsErythemaErythematous plaqueAcral blisteringAbnormality of the kneeRecurrent loss of toenails and fingernailsAbnormality of the elbow
Classification & Codes
Orphanet Code
ORPHA:158673acral dystrophic epidermolysis bullosa
| Orphanet | ORPHA:158673 |
| Treatments | 0 drug(s) |
| Symptoms on record | 20 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO