Disease: Keratosis palmoplantaris striata 3
- 2 Cases of hereditary palmoplantar keratoderma. An abnormality of keratohyalin granules and keratin fibril formation
- Abnormalities of keratinocyte maturation and differentiation in keratosis palmoplantaris striata. Immunohistochemical and ultrastructural study before and during etretinate therapy
- Diffuse nonepidermolytic palmoplantar keratoderma caused by a recurrent nonsense mutation in DSG1
- Disadhesion of epidermal keratinocytes: a histologic clue to palmoplantar keratodermas caused by DSG1 mutations
- Keratoderma palmoplantaris striata
- Whole-exome sequencing analysis reveals co-segregation of a COL20A1 missense mutation in a Pakistani family with striate palmoplantar keratoderma