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Results 1 - 10 of 23 for exercise for children
  1. Glutaric acidemia type II 
    ... Dorland L, Helders P, de Koning T. Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency. ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-ii - Genetics
  2. Very long-chain acyl-CoA dehydrogenase deficiency 
    ... can be triggered by periods of fasting, illness, exercise, and exposure to hot or cold temperatures. In children, this disorder is sometimes mistaken for Reye syndrome, ...
    https://medlineplus.gov/...g-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  3. Anhidrotic ectodermal dysplasia with immune deficiency 
    ... temperature (hyperthermia), particularly in hot weather and during exercise, because the body cannot cool itself by evaporating sweat.The immune deficiency in EDA-ID varies among individuals with this condition. Children with EDA-ID often produce abnormally low levels ...
    https://medlineplus.gov/...todermal-dysplasia-with-immune-deficiency - Genetics
  4. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 
    ... are often triggered by an infection, fasting, strenuous exercise, or other types of stress.HMG-CoA lyase deficiency is sometimes mistaken for Reye syndrome, a severe disorder that develops in children while they appear to be recovering from viral ...
    https://medlineplus.gov/...oxy-3-methylglutaryl-coa-lyase-deficiency - Genetics
  5. MT-TL1 gene 
    ... weakness, pain, and extreme fatigue, particularly during exercise (exercise intolerance). In some cases, the heart muscle is also weakened, which is known as cardiomyopathy. This abnormality prevents the heart from pumping normally.A few children with changes in the MT-TL1 gene have ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  6. Familial restrictive cardiomyopathy 
    ... heart failure. Without treatment, the majority of affected children survive ... to exercise. Some individuals have an irregular heart beat (arrhythmia) ...
    https://medlineplus.gov/.../familial-restrictive-cardiomyopathy - Genetics
  7. Glycogen storage disease type IX 
    ... experience fatigue, muscle pain, and cramps, especially during exercise (exercise intolerance). Most affected individuals have muscle weakness that ... the blood between meals or for energy during exercise. Phosphorylase b kinase turns on (activates) the enzyme ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-ix - Genetics
  8. Mitochondrial complex III deficiency 
    ... weakness (myopathy) and extreme tiredness (fatigue), particularly during exercise (exercise intolerance). More severely affected individuals have problems ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  9. Multiminicore disease 
    ... severe or life-threatening respiratory problems. Almost all children with the ... activity (exercise intolerance). This form accounts for about 10 percent ...
    https://medlineplus.gov/genetics/condition/multiminicore-disease - Genetics
  10. Progressive external ophthalmoplegia 
    ... legs. The weakness may be especially noticeable during exercise (exercise intolerance). Muscle weakness may also cause difficulty swallowing ( ... sperm cells, contribute mitochondria to the developing embryo, children can inherit disorders resulting from mtDNA mutations only ...
    https://medlineplus.gov/.../progressive-external-ophthalmoplegia - Genetics
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