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Can Astigmatism Be A Symptom Of Mitochondrial Disease
A mitochondrial disorder is a condition in which a person has a problem with his mitochondria (small structures inside each cell, that produce energy for the cell). Mitochondria have their own genes, and are passed onto offspring by a different method, compared to the 46 chromosomes from the nucleus (center) of human cells. Yet, mitochondrial disorders ...Read more
Symptoms: Symptoms can be related to anything. Make a list of your symptoms and take them to see your doctor. ...Read more
Chronic fatigue: Mitochondria are the "engines" of the cell. They develop the energy that enables each of your 70 to 100 trilion cells to function. The symptoms are many, depending on how many mitochondria in each cell are genetically affected. ...Read more
My neighbors say my new doctor tends to overdiagnose everyone. He thinks I might have mitochondrial disorder. Can you tell me the symptoms?
Maternal and Regular: A few mitochondrial diseases are passed from the mother to all of her children. This is because certain mitochondrial genes are inherited from the mitochondria in the egg's cytoplasm (outside the "nucleus" that contains the regular genes). Other mitochondrial diseases are inherited the regular way, from the genes in the egg "nucleus" and in the sperm, that code for new mitochondria in the embryo. ...Read moreSee 1 more doctor answer
Genetic change: Mitochondrial diseases can be caused by changes in mitochondrial dna (mtdna), inherited only from mother but most are caused by changes in genes inherited both from mother and father (nuclear genes). It can be inherited in other ways too. More info on the complex inheritance of mitochondrial diseases: http://www.Umdf.Org/site/c.8qkoj0mvf7lug/b.7940911/k.555f/inheritance__genetics.Htm. ...Read more
Often it is: Mitochondrial diseases can present from any organ system at any age. Diagnosis can be made by specific clinical criteria (symptoms, brain MRI imaging, muscle biopsy, elevated lactate in blood) or, by finding a genetic mutation either in mitochondrial dna or one of the hundreds of other genes that cause mitochondrial disease. Latter is a more accurate diagnosis. ...Read more
Hereditary blindness: LHON stands for Leber's hereditary optic neuropathy. It is inherited from mother to child. Usually a young man loses eyesight in the enter of one eye,and shortly after he loses eyesight in other eye. Women are less often affected. Gene mutations that are responsible for this disease is known. There are no curative treatments. If you carry this gene, you should avoid smoking, alcohol certain drugs. ...Read more
Mngie: MNGIE is a multi system autosomal recessive disorder characterized by gastrointestinal dysmotility and peripheral nervous system involvement death occurs before 35 years of life. Treatment options include allogeneic hematopoietic stem cell transplantation and carrier erythrocytes entrapped TP therapy . Hope this answers your question . Mitochondrial Neurogatrointestinal Encephalomyopathy ...Read more
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