Emery-Dreifuss muscular dystrophy 2, autosomal dominant

Emery-Dreifuss muscular dystrophy inherited in an autosomal dominant pattern and caused by mutations in the LMNA gene.

What is Emery-Dreifuss muscular dystrophy 2, autosomal dominant?

Emery-Dreifuss muscular dystrophy 2, autosomal dominant 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 Emery-Dreifuss muscular dystrophy 2, autosomal dominant, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with Emery-Dreifuss muscular dystrophy 2, autosomal dominant

Distal lower limb muscle weaknessDistal upper limb muscle weaknessExertional dyspneaFatigueFoot dorsiflexor weaknessLimb muscle weaknessLimb-girdle muscle weaknessPeroneal muscle weaknessProximal lower limb muscle weaknessProximal upper limb muscle weaknessScapular winging

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.