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Epidermolytic hyperkeratosis, late-onset

MedGen UID:
396272
•Concept ID:
C1862005
•
Disease or Syndrome
Synonym: Epidermolytic Hyperkeratosis, Late-Onset

Recent clinical studies

Etiology

Human keratin diseases: hereditary fragility of specific epithelial tissues.
Corden LD, McLean WH
Exp Dermatol 1996 Dec;5(6):297-307. doi: 10.1111/j.1600-0625.1996.tb00133.x. PMID: 9028791
Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC).
Kelsell DP, Risk JM, Leigh IM, Stevens HP, Ellis A, Hennies HC, Reis A, Weissenbach J, Bishop DT, Spurr NK, Field JK
Hum Mol Genet 1996 Jun;5(6):857-60. doi: 10.1093/hmg/5.6.857. PMID: 8776604

Diagnosis

Human keratin diseases: hereditary fragility of specific epithelial tissues.
Corden LD, McLean WH
Exp Dermatol 1996 Dec;5(6):297-307. doi: 10.1111/j.1600-0625.1996.tb00133.x. PMID: 9028791

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