mitochondrial DNA deletion syndrome with progressive myopathy

mitochondrial DNA deletion syndrome with progressive myopathy is a medical condition that may be associated with various symptoms and signs.

Also known as: mitochondrial DNA deletion syndrome with limb-girdle weakness, mtDNA deletion syndrome with limb-girdle weakness, mtDNA deletion syndrome with progressive myopathy, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 6, PEOA6, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6

Category: General

What is mitochondrial DNA deletion syndrome with progressive myopathy?

mitochondrial DNA deletion syndrome with progressive myopathy 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 mitochondrial DNA deletion syndrome with progressive myopathy, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with mitochondrial DNA deletion syndrome with progressive myopathy

DepressionDyspneaExertional dyspneaMuscle weaknessMyalgiaOphthalmoparesisPelvic girdle muscle weaknessShoulder girdle muscle weakness

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.