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hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome

ORPHA: 79091

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

Hereditary inclusion body myopathy type 3 is characterised by congenital joint contractures (normalizing during early childhood), external ophthalmoplegia, and proximal muscle weakness. In adult cases, the muscular weakness is progressive.

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

Orphanet Code

ORPHA:79091
hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome
OrphanetORPHA:79091
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome | OrphanDrug