progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3

Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the TWNK gene.

What is progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3?

progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3 is a medical condition. A condition is a disease, disorder, or abnormal state that affects the body or mind. This page provides educational information only and is not a diagnosis.

If you think you may have progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3

DepressionDysphagiaFatigueLimb muscle weaknessMyalgiaProgressive hearing impairmentProgressive muscle weaknessProximal muscle weaknessSeizure

When to seek medical care

Seek medical advice if you have symptoms that are severe, persistent, or affecting your daily life. Emergency care is needed for symptoms like chest pain, difficulty breathing, confusion, or severe weakness.