coenzyme Q10 deficiency, primary, 1
Any coenzyme Q10 deficiency in which the cause of the disease is a mutation in the COQ2 gene.
Also known as: COQ2 coenzyme Q10 deficiency, coenzyme Q10 deficiency caused by mutation in COQ2, coenzyme Q10 deficiency, primary, 1, coenzyme Q10 deficiency, primary, type 1, COQ10D1.
Category: General
Symptoms associated with coenzyme Q10 deficiency, primary, 1
The following symptoms have been associated with coenzyme Q10 deficiency, primary, 1 in medical literature. Not everyone experiences the same symptoms.
Dysphagia
Difficulty in swallowing....
Episodic vomiting
Paroxysmal, recurrent episodes of vomiting....
Fatigue
A subjective feeling of tiredness characterized by a lack of energy and motivation....
Progressive muscle weakness
Information about Progressive muscle weakness....
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Sensorineural hearing impairment
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve....
Status epilepticus
Status epilepticus is a type of prolonged seizure resulting either from the failure of the mechanisms responsi...
Tremor
An unintentional, oscillating to-and-fro muscle movement about a joint axis....
Visual loss
Loss of visual acuity (implying that vision was better at a certain time point in life). Otherwise the term re...
Tests used to investigate coenzyme Q10 deficiency, primary, 1
Healthcare providers may order these tests when evaluating coenzyme Q10 deficiency, primary, 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 coenzyme Q10 deficiency, primary, 1, which is why a clinical evaluation is important.
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Frequently Asked Questions
What is coenzyme Q10 deficiency, primary, 1?
coenzyme Q10 deficiency, primary, 1 is a health condition described in medical literature. Any coenzyme Q10 deficiency in which the cause of the disease is a mutation in the COQ2 gene.
What are the symptoms of coenzyme Q10 deficiency, primary, 1?
coenzyme Q10 deficiency, primary, 1 is associated with 9 symptoms in the medical literature we index, including Dysphagia, Episodic vomiting, Fatigue, Progressive muscle weakness, Seizure, Sensorineural hearing impairment. Symptoms vary widely between individuals.
How is coenzyme Q10 deficiency, primary, 1 diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with coenzyme Q10 deficiency, primary, 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 coenzyme Q10 deficiency, primary, 1, please discuss your symptoms with a qualified healthcare provider.