Article

A rare report of cardiofaciocutaneous syndrome and ulerythema ophryogenes

2023-04-11

Abstract excerpt

Cardiofaciocutaneous syndrome is a rare genetic disorder. It is characterized by craniofacial dysmorphism, congenital heart disease, ectodermal abnormalities, developmental delay, and central nervous system disorders. We discuss the case of an 11-year-old boy with cardiofaciocutaneous syndrome presenting with ulerythema ophryogenes and phenotypic features similar to Noonan syndrome.

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Literature Corpus work: d1d52e5c-4f8b-5b12-a86b-769e684c3150
DOI: 10.22541/au.168120021.10517033/v1

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