A rare report of cardiofaciocutaneous syndrome and ulerythema ophryogenes

Maryam Sadat Sadati; Zeinab Bizaval; mitra abdolvand; Mohammad Reza khalili

doi:10.22541/au.168120021.10517033/v1

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A rare report of cardiofaciocutaneous syndrome and ulerythema ophryogenes

Maryam Sadat Sadati,
Zeinab Bizaval,
mitra abdolvand,
Mohammad Reza khalili

Abstract

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.

31 Mar 2023Submitted to Clinical Case Reports

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11 Apr 2023Submission Checks Completed

11 Apr 2023Assigned to Editor

14 Apr 2023Reviewer(s) Assigned

25 Apr 2023Review(s) Completed, Editorial Evaluation Pending

25 Apr 2023Editorial Decision: Revise Minor

Abstract

Peer review status:IN REVISION