congenital myopathy 23

Any nemaline myopathy in which the cause of the disease is a mutation in the TPM2 gene.

Also known as: CAPM2, NEM4, TPM2 nemaline myopathy, nemaline myopathy 4, nemaline myopathy caused by mutation in TPM2, nemaline myopathy type 4

Category: General

What is congenital myopathy 23?

congenital myopathy 23 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 23, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with congenital myopathy 23

DysphagiaExercise-induced myalgiaFacial diplegiaFatigueLimb muscle weaknessLower limb muscle weaknessNeck muscle weaknessProximal muscle weaknessScapular wingingSeizure

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.