Understanding Sclerodactyly: Causes, Symptoms, and Treatment Options

Sclerodactyly is a rare genetic disorder that affects the development of the hands and feet. It is characterized by thickening and hardening of the skin on the fingers and toes, as well as other symptoms such as joint contractures and limited mobility. The condition is usually inherited in an autosomal dominant pattern, meaning that a single copy of the mutated gene is enough to cause the condition. Treatment for sclerodactyly typically involves physical therapy and occupational therapy to improve joint mobility and strength, as well as surgery to release contracted tendons and improve hand function.

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