congenital myopathy 22A, classic
congenital myopathy 22A, classic is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with congenital myopathy 22A, classic
The following symptoms have been associated with congenital myopathy 22A, classic in medical literature. Not everyone experiences the same symptoms.
Axial muscle weakness
Reduced strength of the axial musculature (i.e., of the muscles of the head and neck, spine, and ribs)....
Deeply set eye
An eye that is more deeply recessed into the plane of the face than is typical....
External ophthalmoplegia
Paralysis of the external ocular muscles....
Fatigue
A subjective feeling of tiredness characterized by a lack of energy and motivation....
Generalized muscle weakness
Generalized weakness or decreased strength of the muscles, affecting both distal and proximal musculature....
Limb muscle weakness
Reduced strength and weakness of the muscles of the arms and legs....
Proximal lower limb muscle weakness
A lack of strength of the proximal muscles of the legs....
Scapular winging
Abnormal protrusion of the scapula away from the surface of the back....
Weakness of facial musculature
Reduced strength of one or more muscles innervated by the facial nerve (the seventh cranial nerve)....
Tests used to investigate congenital myopathy 22A, classic
Healthcare providers may order these tests when evaluating congenital myopathy 22A, classic. 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 22A, classic, which is why a clinical evaluation is important.
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Autosomal dominant progressive external ophthalmoplegia
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Emery-Dreifuss muscular dystrophy 2, autosomal dominant
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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 22A, classic?
congenital myopathy 22A, classic is a health condition described in medical literature. congenital myopathy 22A, classic is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of congenital myopathy 22A, classic?
congenital myopathy 22A, classic is associated with 9 symptoms in the medical literature we index, including Axial muscle weakness, Deeply set eye, External ophthalmoplegia, Fatigue, Generalized muscle weakness, Limb muscle weakness. Symptoms vary widely between individuals.
How is congenital myopathy 22A, classic diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with congenital myopathy 22A, classic 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 22A, classic, please discuss your symptoms with a qualified healthcare provider.