progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6 is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6
The following symptoms have been associated with progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6 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)....
Dysphagia
Difficulty in swallowing....
Limb muscle weakness
Reduced strength and weakness of the muscles of the arms and legs....
Nausea
A sensation of unease in the stomach together with an urge to vomit....
Sensorineural hearing impairment
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve....
Vomiting
Forceful ejection of the contents of the stomach through the mouth by means of a series of involuntary spasmic...
Weakness of facial musculature
Reduced strength of one or more muscles innervated by the facial nerve (the seventh cranial nerve)....
Tests used to investigate progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6
Healthcare providers may order these tests when evaluating progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6. 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 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6, which is why a clinical evaluation is important.
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congenital myopathy 10b, mild variant
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multiple mitochondrial dysfunctions syndrome 9b
A mitochondrial dysfunction syndrome in which the cause of the disease is a mutation in the FDXR gene. It is c...
oculopharyngodistal myopathy 3
oculopharyngodistal myopathy 3 is a medical condition that may be associated with various symptoms and signs....
Frequently Asked Questions
What is progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6?
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6 is a health condition described in medical literature. progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6 is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6?
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6 is associated with 7 symptoms in the medical literature we index, including Axial muscle weakness, Dysphagia, Limb muscle weakness, Nausea, Sensorineural hearing impairment, Vomiting. Symptoms vary widely between individuals.
How is progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6 diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6 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 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6, please discuss your symptoms with a qualified healthcare provider.