nemaline myopathy 5C, autosomal dominant
nemaline myopathy 5C, autosomal dominant is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with nemaline myopathy 5C, autosomal dominant
The following symptoms have been associated with nemaline myopathy 5C, autosomal dominant in medical literature. Not everyone experiences the same symptoms.
Dysphagia
Difficulty in swallowing....
Foot dorsiflexor weakness
Weakness of the muscles responsible for dorsiflexion of the foot, that is, of the movement of the toes towards...
Lower limb muscle weakness
Weakness of the muscles of the legs....
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 ...
Proximal muscle weakness
A lack of strength of the proximal muscles....
Quadriceps muscle weakness
Weakness of the quadriceps muscle (that is, of the muscle fasciculus of quadriceps femoris)....
Scapular winging
Abnormal protrusion of the scapula away from the surface of the back....
Shoulder girdle muscle weakness
The shoulder, or pectoral, girdle is composed of the clavicles and the scapulae. Shoulder-girdle weakness refe...
Weakness of facial musculature
Reduced strength of one or more muscles innervated by the facial nerve (the seventh cranial nerve)....
Tests used to investigate nemaline myopathy 5C, autosomal dominant
Healthcare providers may order these tests when evaluating nemaline myopathy 5C, 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 nemaline myopathy 5C, autosomal dominant, which is why a clinical evaluation is important.
Congenital fiber-type disproportion myopathy
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Distal myotilinopathy
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Pure mitochondrial myopathy
Pure mitochondrial myopathy is a medical condition that may be associated with various symptoms and signs....
Steinert myotonic dystrophy
Steinert myotonic dystrophy is a medical condition that may be associated with various symptoms and signs....
myofibrillar myopathy 2
Any autosomal dominant distal myopathy in which the cause of the disease is a mutation in the CRYAB gene....
myopathy, myofibrillar, 9, with early respiratory failure
myopathy, myofibrillar, 9, with early respiratory failure is a medical condition that may be associated with v...
Frequently Asked Questions
What is nemaline myopathy 5C, autosomal dominant?
nemaline myopathy 5C, autosomal dominant is a health condition described in medical literature. nemaline myopathy 5C, autosomal dominant is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of nemaline myopathy 5C, autosomal dominant?
nemaline myopathy 5C, autosomal dominant is associated with 9 symptoms in the medical literature we index, including Dysphagia, Foot dorsiflexor weakness, Lower limb muscle weakness, Pelvic girdle muscle weakness, Proximal muscle weakness, Quadriceps muscle weakness. Symptoms vary widely between individuals.
How is nemaline myopathy 5C, autosomal dominant diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with nemaline myopathy 5C, 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 nemaline myopathy 5C, autosomal dominant, please discuss your symptoms with a qualified healthcare provider.