A rare report of cardiofaciocutaneous syndrome and ulerythema
ophryogenes
- Maryam Sadat Sadati
, - Zeinab Bizaval,
- mitra abdolvand,
- Mohammad Reza khalili
Mohammad Reza khalili
Shiraz University of Medical Sciences
Author ProfileAbstract
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 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
