childhood type dermatomyositis
ORPHA: 93672
Overview
Human disease
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 childhood type dermatomyositis, sourced from HPO and Orphanet clinical annotations.
Dry skinSkin rashPruritusCutaneous photosensitivityPoikilodermaHypotoniaDysarthriaMuscle weaknessArthritisLimitation of joint mobilityAlopeciaHoarse voiceDysphoniaCardiomyopathyAngina pectorisPericarditisWeight lossFeverDysphagiaConstipationAbdominal painRestrictive ventilatory defectDyspneaPulmonary fibrosisGastrointestinal hemorrhageVasculitisArthralgiaAutoimmunityElevated circulating creatine kinase concentrationMyalgiaMuscle spasmEMG abnormalityElevated erythrocyte sedimentation rateCalcinosisErythemaElevated circulating C-reactive protein concentrationArrhythmiaBundle branch blockFatigueCoughPalpebral edemaMucosal telangiectasiaeTelangiectasia of the skinMyositisSkin ulcer
Classification & Codes
Orphanet Code
ORPHA:93672childhood type dermatomyositis
| Orphanet | ORPHA:93672 |
| Treatments | 0 drug(s) |
| Symptoms on record | 45 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO