CMT AND NEUROGENIC DISEASE

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Lipodystrophies are a group of rare disorders characterized by variable loss of body fat and insulin resistance–related metabolic complications. Lipodystrophies can be classified as acquired and hereditary by their etiology. They are also classified as localized, partial or generalized in respect to the fat loss distribution. Neuromuscular involvements such as polyneuropathy, hypertrophic appearance in muscles and myopathy have been reported in lipodystrophies. Herein, we present two siblings with familial partial lipodystrophy.

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