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, SPMM, autosomal dominant myosin storage myopathy, myopathy with lysis of type 1 myofibrils, myopathy, hyaline body, autosomal dominant.
Category: General
Symptoms associated with congenital myopathy 7A, myosin storage, autosomal dominant
The following symptoms have been associated with congenital myopathy 7A, myosin storage, autosomal dominant in medical literature. Not everyone experiences the same symptoms.
Generalized muscle weakness
Generalized weakness or decreased strength of the muscles, affecting both distal and proximal musculature....
Muscle weakness
Reduced strength of muscles....
Neck flexor weakness
Weakness of the muscles involved in neck flexion (sternocleidomastoid, longus capitus, longus colli, and scale...
Pelvic girdle muscle weakness
Weakness of the muscles of the pelvic girdle (also known as the hip girdle), that is, lack of strength of the ...
Scapular winging
Abnormal protrusion of the scapula away from the surface of the back....
Scapuloperoneal weakness
Information about Scapuloperoneal weakness....
Shoulder girdle muscle weakness
The shoulder, or pectoral, girdle is composed of the clavicles and the scapulae. Shoulder-girdle weakness refe...
Tests used to investigate congenital myopathy 7A, myosin storage, autosomal dominant
Healthcare providers may order these tests when evaluating congenital myopathy 7A, myosin storage, autosomal dominant. 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 7A, myosin storage, autosomal dominant, which is why a clinical evaluation is important.
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Pure mitochondrial myopathy
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Steinert myotonic dystrophy
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myopathy, myofibrillar, 9, with early respiratory failure
myopathy, myofibrillar, 9, with early respiratory failure is a medical condition that may be associated with v...
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
A rare mitochondrial disease characterized by adult onset of the triad of sensory ataxic neuropathy, dysarthri...
Frequently Asked Questions
What is congenital myopathy 7A, myosin storage, autosomal dominant?
congenital myopathy 7A, myosin storage, autosomal dominant is a health condition described in medical literature. congenital myopathy 7A, myosin storage, autosomal dominant is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of congenital myopathy 7A, myosin storage, autosomal dominant?
congenital myopathy 7A, myosin storage, autosomal dominant is associated with 7 symptoms in the medical literature we index, including Generalized muscle weakness, Muscle weakness, Neck flexor weakness, Pelvic girdle muscle weakness, Scapular winging, Scapuloperoneal weakness. Symptoms vary widely between individuals.
How is congenital myopathy 7A, myosin storage, autosomal dominant diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with congenital myopathy 7A, myosin storage, autosomal dominant 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 7A, myosin storage, autosomal dominant, please discuss your symptoms with a qualified healthcare provider.