progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
Any autosomal dominant progressive external ophthalmoplegia in which the cause of the disease is a mutation in the POLG gene.
Also known as: PEOA1, POLG autosomal dominant progressive external ophthalmoplegia, autosomal dominant progressive external ophthalmoplegia caused by mutation in POLG, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1, progressive external ophthalmoplegia, autosomal dominant 1.
Category: General
Symptoms associated with progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
The following symptoms have been associated with progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 in medical literature. Not everyone experiences the same symptoms.
Depression
Frequently experiencing feelings of being down, miserable, and/or hopeless; struggling to recover from these m...
Diplopia
Diplopia is a condition in which a single object is perceived as two images, it is also known as double vision...
Dysphagia
Difficulty in swallowing....
Facial palsy
Facial nerve palsy is a dysfunction of cranial nerve VII (the facial nerve) that results in inability to contr...
Hand tremor
An unintentional, oscillating to-and-fro muscle movement affecting the hand....
Limb muscle weakness
Reduced strength and weakness of the muscles of the arms and legs....
Neck flexor weakness
Weakness of the muscles involved in neck flexion (sternocleidomastoid, longus capitus, longus colli, and scale...
Progressive muscle weakness
Information about Progressive muscle weakness....
Resting tremor
A resting tremor occurs when muscles are at rest and becomes less noticeable or disappears when the affected m...
Sensorineural hearing impairment
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve....
Tests used to investigate progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
Healthcare providers may order these tests when evaluating progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1. 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 dominant 1, which is why a clinical evaluation is important.
Alexander disease
Alexander disease is a medical condition that may be associated with various symptoms and signs....
Autosomal dominant progressive external ophthalmoplegia
Autosomal dominant progressive external ophthalmoplegia is a medical condition that may be associated with var...
Full NF2-related schwannomatosis
Full NF2-related schwannomatosis is a medical condition that may be associated with various symptoms and signs...
Morimoto-Ryu-Malicdan neuromuscular syndrome
Morimoto-Ryu-Malicdan neuromuscular syndrome is a medical condition that may be associated with various sympto...
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
Any autosomal recessive progressive external ophthalmoplegia in which the cause of the disease is a mutation i...
spinocerebellar ataxia 52
spinocerebellar ataxia 52 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 dominant 1?
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 is a health condition described in medical literature. Any autosomal dominant progressive external ophthalmoplegia in which the cause of the disease is a mutation in the POLG gene.
What are the symptoms of progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1?
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 is associated with 10 symptoms in the medical literature we index, including Depression, Diplopia, Dysphagia, Facial palsy, Hand tremor, Limb muscle weakness. Symptoms vary widely between individuals.
How is progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 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 dominant 1 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 dominant 1, please discuss your symptoms with a qualified healthcare provider.