progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4

Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the POLG2 gene.

Also known as: POLG2 progressive external ophthalmoplegia with mitochondrial DNA deletions, progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in POLG2, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 4, PEOA4

Category: General

What is progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4?

progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4 is a recognized medical condition. This page explains what it is, symptoms that may accompany it, and the lab tests healthcare providers sometimes use to investigate it. It is educational information only and is not a diagnosis.

If you think you may have progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4, 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 4

ConstipationFacial palsyFailure to thriveGastroesophageal refluxLimb muscle weaknessMyalgiaProgressive 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.