This is a specific genetic syndrome distinguished by the fusion of the eyelids (ankyloblepharon), cleft lip/palate, and ectodermal defects, in addition to skin fragility.
This form of ichthyosis presents at birth with erythroderma and blistering, but the predominant feature becomes hyperkeratosis and scaling as the child ages, unlike the primary blistering of EB.
Also known as congenital erythropoietic porphyria, this is a metabolic disorder of porphyrin synthesis, distinguished by red-colored urine, photosensitivity, and hemolytic anemia.
This is a superficial form of epidermolytic ichthyosis, distinguished by its characteristic "molting" or peeling of grayish scale, a feature not seen in EB.
Also known as erythrodermia with palmoplantar keratoderma, it is distinguished by the prominent thickening of palms and soles, which is not a defining feature of all EB types.
