Carnitine deficiency is an autosomal recessive genetic disease, but can also be caused by other diseases (secondary).There is a big variety causes and symptoms in severity and nature. There is a form where the shortage of carnitine occurs only in the muscles (myopathic form) and a form where it also occurs in other organs (systemic form). The myopathic form is very rare. The first symptoms of muscle weakness can occur in early childhood. It is a general weakness involving the proximal muscles (near the trunk) more affected than distal muscles (further away from the trunk). The facial muscles may be affected.Central to the treatment of all forms is the administration of carnitine to overcome the deficit and its consequences.
Lily has no effect on other symptoms or progression of any disease. Note: Results may vary depending on the nature, cause and severity of the ptosis and the way Lily is applied.
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