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Epidermal hyperkeratosis
- ... KRT1 gene mutations are associated with PS-type epidermal hyperkeratosis, and KRT10 gene mutations are usually associated with ...
- ... to their premature death. The mechanisms by which epidermal damage and cell death contribute to hyperkeratosis at erythematous areas are poorly understood. More About ...
- ... types of gap junctions. The mechanisms by which epidermal damage and cell death contribute to hyperkeratosis and erythematous areas are poorly understood. More About ...
- ... death in the epidermis. The mechanisms by which epidermal damage and cell death contribute to hyperkeratosis and erythematous areas are poorly understood.Mutations in ...
- ... palmoplantar hyperkeratosis with detachment or loosening of the epidermis (epidermolysis), usually seen as blistering. People with nonepidermolytic palmoplantar keratoderma have palmoplantar hyperkeratosis with no evidence of epidermolysis. In striate palmoplantar ...
- ... with changes in mtDNA to their children. Palmoplantar hyperkeratosis-deafness syndrome Palmoplantar hyperkeratosis-hearing loss syndrome Palmoplantar ...
- The KRT10 gene provides instructions for making a protein called keratin 10. Keratins are a group of tough, fibrous proteins that form the structural framework ...
- ... leukonychia syndrome Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome National Organization for Rare Disorders (NORD) BART- ...
- ... and soles of the feet thickens and hardens (hyperkeratosis). Kindler EB can also cause people to be ... found in the outer layer of skin (the epidermis) and in the mucosae. In people with Kindler ...
- ... to the outer layer of the skin (the epidermis). Mutations in either the KRT5 or KRT14 gene ... assembling into strong networks, causing cells in the epidermis to become fragile and easily damaged. As a ...