Abstract
Muir-Torre syndrome, a variant of Lynch syndrome or hereditary nonpolyposis colorectal cancer, is an autosomal dominant disease characterized by skin neoplasms (sebaceous or keratoacanthomas) and visceral malignancies. Due to the rarity of the syndrome there are no firm guidelines on how and when to test patients with its typical skin lesions. We describe a case that highlights the importance of a detailed family history.
Original language | English (US) |
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Pages (from-to) | 180-185 |
Number of pages | 6 |
Journal | Case Reports in Ophthalmology |
Volume | 10 |
Issue number | 2 |
DOIs | |
State | Published - May 1 2019 |
Keywords
- Enzyme replacement therapy
- Hunter syndrome
- Idursulfase
- Mucopolysaccharidosis type II
- Recovery
- Vision
ASJC Scopus subject areas
- Ophthalmology