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</html><description>The original name for this disorder was toxopachyosteose diaphysaire tibio-peroniere. Weismann Netter Stuhl syndrome is an extremely rare skeletal disorder that occurs as the result of abnormal development of the bone. This disorder, also referred to as dwarfism, is thought to be inherited as an autosomal or X-linked dominant genetic trait.</description></oembed>
