myopathy, distal, 7, adult-onset, X-linked
myopathy, distal, 7, adult-onset, X-linked is a medical condition that may be associated with various symptoms and signs.
Also known as: MPD7, myopathy, distal, 7, adult-onset, X-linked.
Category: General
Symptoms associated with myopathy, distal, 7, adult-onset, X-linked
The following symptoms have been associated with myopathy, distal, 7, adult-onset, X-linked in medical literature. Not everyone experiences the same symptoms.
Distal lower limb muscle weakness
Reduced strength of the distal musculature of the legs....
Distal upper limb muscle weakness
Reduced strength of the distal musculature of the arms....
Hearing impairment
A decreased magnitude of the sensory perception of sound....
Proximal lower limb muscle weakness
A lack of strength of the proximal muscles of the legs....
Proximal upper limb muscle weakness
A lack of strength of the proximal muscles of the arms....
Respiratory insufficiency due to muscle weakness
Information about Respiratory insufficiency due to muscle weakness....
Scapular winging
Abnormal protrusion of the scapula away from the surface of the back....
Tests used to investigate myopathy, distal, 7, adult-onset, X-linked
Healthcare providers may order these tests when evaluating myopathy, distal, 7, adult-onset, X-linked. 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 myopathy, distal, 7, adult-onset, X-linked, which is why a clinical evaluation is important.
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Autosomal dominant Charcot-Marie-Tooth disease type 2Z
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Charcot-Marie-tooth disease, axonal, type 2JJ
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Emery-Dreifuss muscular dystrophy 2, autosomal dominant
Emery-Dreifuss muscular dystrophy inherited in an autosomal dominant pattern and caused by mutations in the LM...
congenital myopathy 25
congenital myopathy 25 is a medical condition that may be associated with various symptoms and signs....
myopathy, myofibrillar, 13, with rimmed vacuoles
A rare genetic neuromuscular disease caused by a mutation in HSPB8 gene, characterized by length-dependent axo...
Frequently Asked Questions
What is myopathy, distal, 7, adult-onset, X-linked?
myopathy, distal, 7, adult-onset, X-linked is a health condition described in medical literature. myopathy, distal, 7, adult-onset, X-linked is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of myopathy, distal, 7, adult-onset, X-linked?
myopathy, distal, 7, adult-onset, X-linked is associated with 7 symptoms in the medical literature we index, including Distal lower limb muscle weakness, Distal upper limb muscle weakness, Hearing impairment, Proximal lower limb muscle weakness, Proximal upper limb muscle weakness, Respiratory insufficiency due to muscle weakness. Symptoms vary widely between individuals.
How is myopathy, distal, 7, adult-onset, X-linked diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with myopathy, distal, 7, adult-onset, X-linked 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 myopathy, distal, 7, adult-onset, X-linked, please discuss your symptoms with a qualified healthcare provider.