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Congenital ichthyosiform erythroderma, also known as nonbullous congenital ichthyosiform erythroderma,: 484  is a rare type of the ichthyosis family of...

Townes–Brocks syndrome (TBS) is a rare genetic disease that has been described in approximately 200 cases in the published literature. It affects both...

Holocarboxylase synthetase deficiency is an inherited metabolic disorder in which the body is unable to use the vitamin biotin effectively. This disorder...