autosomal dominant progressive external ophthalmoplegia

Autosomal dominant progressive external ophthalmoplegia is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

The condition is characterized by progressive external ophthalmoplegia and is associated with mitochondrial DNA deletions. It is classified as an autosomal dominant disorder, although specific inheritance patterns and symptoms have not been detailed in the available data.

Patients and caregivers are encouraged to seek genetic counseling to understand the implications of this inherited condition. Connecting with rare disease registries such as Orphanet may provide additional resources and support. Finding specialists experienced with mitochondrial disorders can also be beneficial.