muscular dystrophy, limb-girdle, autosomal recessive 29
muscular dystrophy, limb-girdle, autosomal recessive 29 is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with muscular dystrophy, limb-girdle, autosomal recessive 29
The following symptoms have been associated with muscular dystrophy, limb-girdle, autosomal recessive 29 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)....
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....
Hand muscle weakness
Reduced strength of the musculature of the hand....
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....
Sensorineural hearing impairment
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve....
Weakness of facial musculature
Reduced strength of one or more muscles innervated by the facial nerve (the seventh cranial nerve)....
Tests used to investigate muscular dystrophy, limb-girdle, autosomal recessive 29
Healthcare providers may order these tests when evaluating muscular dystrophy, limb-girdle, autosomal recessive 29. 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 muscular dystrophy, limb-girdle, autosomal recessive 29, which is why a clinical evaluation is important.
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Charcot-Marie-Tooth disease type 1F
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Charcot-Marie-Tooth disease type 4B2
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congenital myopathy 25
congenital myopathy 25 is a medical condition that may be associated with various symptoms and signs....
oculopharyngodistal myopathy 5
oculopharyngodistal myopathy 5 is a medical condition that may be associated with various symptoms and signs....
Frequently Asked Questions
What is muscular dystrophy, limb-girdle, autosomal recessive 29?
muscular dystrophy, limb-girdle, autosomal recessive 29 is a health condition described in medical literature. muscular dystrophy, limb-girdle, autosomal recessive 29 is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of muscular dystrophy, limb-girdle, autosomal recessive 29?
muscular dystrophy, limb-girdle, autosomal recessive 29 is associated with 8 symptoms in the medical literature we index, including Axial muscle weakness, Distal lower limb muscle weakness, Distal upper limb muscle weakness, Hand muscle weakness, Proximal lower limb muscle weakness, Proximal upper limb muscle weakness. Symptoms vary widely between individuals.
How is muscular dystrophy, limb-girdle, autosomal recessive 29 diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with muscular dystrophy, limb-girdle, autosomal recessive 29 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 muscular dystrophy, limb-girdle, autosomal recessive 29, please discuss your symptoms with a qualified healthcare provider.