Tylosis

Overview

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Articles
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Evidence Based Medicine
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Guidelines / Policies / Govt
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Continuing Medical Education (CME)
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List of terms related to Tylosis

Tylosis is an autosomal dominant disorder. In tylosis, there is hyperkeratinization of palms and soles. Though a rare disease, it is known to predispose to squamous cell carcinoma of the esophagus.

Tylosis is inherited in an autosomal dominant fashion.

See also

• Howel-Evans syndrome

External links

• Online Mendelian Inheritance in Man (OMIM) 148500
• Photo
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• PMID 9609757 "Tylosis esophageal cancer locus on chromosome 17q25.1 is commonly deleted in sporadic human esophageal cancer."