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
Symptoms associated with congenital myopathy 23
The following symptoms have been associated with congenital myopathy 23 in medical literature. Not everyone experiences the same symptoms.
Dysphagia
Difficulty in swallowing....
Exercise-induced myalgia
The occurrence of an unusually high amount of muscle pain following exercise....
Facial diplegia
Facial diplegia refers to bilateral facial palsy (bilateral facial palsy is much rarer than unilateral facial ...
Fatigue
A subjective feeling of tiredness characterized by a lack of energy and motivation....
Limb muscle weakness
Reduced strength and weakness of the muscles of the arms and legs....
Lower limb muscle weakness
Weakness of the muscles of the legs....
Neck muscle weakness
Decreased strength of the neck musculature....
Proximal muscle weakness
A lack of strength of the proximal muscles....
Scapular winging
Abnormal protrusion of the scapula away from the surface of the back....
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Tests used to investigate congenital myopathy 23
Healthcare providers may order these tests when evaluating congenital myopathy 23. Test selection is a clinical decision made by a qualified professional.
CBC with Differential
Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...
Comprehensive Metabolic Panel (CMP)
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...
Urinalysis
Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....
Conditions with overlapping symptoms
These conditions share symptoms with congenital myopathy 23, which is why a clinical evaluation is important.
Autosomal dominant Charcot-Marie-Tooth disease type 2Z
Autosomal dominant Charcot-Marie-Tooth disease type 2Z is a medical condition that may be associated with vari...
Autosomal dominant progressive external ophthalmoplegia
Autosomal dominant progressive external ophthalmoplegia is a medical condition that may be associated with var...
Morimoto-Ryu-Malicdan neuromuscular syndrome
Morimoto-Ryu-Malicdan neuromuscular syndrome is a medical condition that may be associated with various sympto...
Steinert myotonic dystrophy
Steinert myotonic dystrophy is a medical condition that may be associated with various symptoms and signs....
multiple mitochondrial dysfunctions syndrome 9b
A mitochondrial dysfunction syndrome in which the cause of the disease is a mutation in the FDXR gene. It is c...
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is...
Frequently Asked Questions
What is congenital myopathy 23?
congenital myopathy 23 is a health condition described in medical literature. Any nemaline myopathy in which the cause of the disease is a mutation in the TPM2 gene.
What are the symptoms of congenital myopathy 23?
congenital myopathy 23 is associated with 10 symptoms in the medical literature we index, including Dysphagia, Exercise-induced myalgia, Facial diplegia, Fatigue, Limb muscle weakness, Lower limb muscle weakness. Symptoms vary widely between individuals.
How is congenital myopathy 23 diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with congenital myopathy 23 include CBC with Differential, Comprehensive Metabolic Panel (CMP), Urinalysis. This information is educational, not a diagnosis.
Is SymptomDatabase.com diagnosing me?
No. SymptomDatabase.com does not provide diagnosis. If you are concerned you may have congenital myopathy 23, please discuss your symptoms with a qualified healthcare provider.