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

Corresponding Author:[email protected]

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Zeinab Bizaval
Shiraz University of Medical Sciences
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mitra abdolvand
Shiraz University of Medical Sciences
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Mohammad Reza khalili
Shiraz University of Medical Sciences
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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
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