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Skin disorder
- Peeling skin syndrome 2 is a skin disorder characterized by painless peeling of the top layer of skin. In this form of peeling skin syndrome, the peeling is most apparent ...
- ... psoriasis (GPP) is a severe form of a skin disorder called psoriasis. GPP and other forms of psoriasis ... IL1F5 are associated with the severe episodic inflammatory skin disease known as generalized pustular psoriasis. Am J Hum ...
- Epidermolytic hyperkeratosis is a skin disorder that is present at birth. Affected babies may have very red skin (erythroderma) and severe blisters. Because newborns with this ...
- Mal de Meleda is a rare skin disorder that begins in early infancy. Affected individuals have a condition known as palmoplantar keratoderma, in which the skin of the palms of ...
- Erythrokeratodermia variabilis et progressiva (EKVP) is a skin disorder that is present at birth or becomes apparent in infancy. Although its signs and symptoms vary, the condition is characterized by two major ...
- Steatocystoma multiplex is a skin disorder characterized by the development of multiple noncancerous (benign) cysts known as steatocystomas. These growths begin in the skin's sebaceous ...
- ... arthritis) that usually occurs in combination with a skin disorder called psoriasis. Psoriasis is a chronic inflammatory condition characterized by patches of red, irritated skin that are often covered by flaky white scales. ...
- ... people with epidermolytic hyperkeratosis. This condition is a skin disorder characterized by red, blistering skin at an early ... KRT1 gene mutations are involved in many other skin disorders. In several of these conditions, there is palmoplantar ...
- ... and hidradenitis suppurativa is sometimes misdiagnosed as other skin disorders.In some families, including those with an NCSTN, ... Registry: Familial acne inversa ... Epub 2010 Oct 7. Citation on PubMed
- ... Mutations in the KRT10 gene can cause another skin disorder known as ichthyosis with confetti (also called congenital ... Condition Cyclic ichthyosis with epidermolytic hyperkeratosis is another skin disorder caused by mutations in the KRT10 gene. This ...
