Oculopharyngodistal myopathy
MeSH: C563508ORPHA: 98897
Overview
medical condition
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 Oculopharyngodistal myopathy, sourced from HPO and Orphanet clinical annotations.
Gait disturbanceAbnormality of facial musculatureProgressive external ophthalmoplegiaOphthalmoparesisWeight lossProgressive ptosisNasal dysarthriaWeakness of facial musculatureTongue muscle weaknessHigh palateVocal cord paresisMyopathic faciesRecurrent aspiration pneumoniaHigh, narrow palateRespiratory insufficiency due to muscle weaknessDistal upper limb amyotrophyBowing of the vocal cordsDistal lower limb amyotrophyDistal lower limb muscle weaknessProgressive distal muscle weaknessImpaired oropharyngeal swallow responseOral-pharyngeal dysphagiaAbnormal morphology of musculature of pharynxProgressive sensorineural hearing impairmentAreflexiaRestrictive ventilatory defectLoss of ambulationDistal upper limb muscle weaknessTibialis muscle weaknessFoot dorsiflexor weaknessProgressive proximal muscle weaknessFatigable weakness of bulbar musclesAbnormality of masseter muscleProximal upper limb muscle weaknessParaplegiaAbnormality of orbicularis oris muscle
Classification & Codes
MeSH Code
C563508Orphanet Code
ORPHA:98897Oculopharyngodistal myopathy
| MeSH | C563508 |
| Orphanet | ORPHA:98897 |
| Treatments | 0 drug(s) |
| Symptoms on record | 36 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO