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Up to: Syndromic disease · Focal palmoplantar keratoderma
Palmoplantar keratoderma-esophageal carcinoma syndrome
An inherited condition characterized by palmoplantar keratoderma and esophageal cancer. The palmoplantar keratoderma usually begins around age 10, and esophageal cancer may form after age 20. This condition is caused by a mutation in the RHBDF2 gene and is inherited in an autosomal dominant pattern.
This condition has no sub-types.