congenital myopathy 7A, myosin storage, autosomal dominant

congenital myopathy 7A, myosin storage, autosomal dominant is a medical condition that may be associated with various symptoms and signs.

Also known as: MSMA, MYH7-related late-onset SPMD, MYH7-related late-onset scapuloperoneal muscular dystrophy, MYH7-related late-onset scapuloperoneal syndrome, MYH7-related scapuloperoneal myopathy, SPMD

Category: General

What is congenital myopathy 7A, myosin storage, autosomal dominant?

congenital myopathy 7A, myosin storage, autosomal dominant 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 congenital myopathy 7A, myosin storage, autosomal dominant, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with congenital myopathy 7A, myosin storage, autosomal dominant

Generalized muscle weaknessMuscle weaknessNeck flexor weaknessPelvic girdle muscle weaknessScapular wingingScapuloperoneal 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.