Literature DB >> 24605344

Ulerythema ophryogenes: updates and insights.

Christopher M Morton, Chinmoy Bhate, Camila K Janniger, Robert A Schwartz1.   

Abstract

Ulerythema ophryogenes is a rare cutaneous atrophic disorder that occasionally is associated with Noonan syndrome, de Lange syndrome, Rubinstein-Taybi syndrome, and cardiofaciocutaneous (CFC) syndrome. Often presenting in pediatric patients, the pathogenesis of ulerythema ophryogenes remains unclear, though several genetic causes have been suggested. Treatment recommendations remain anecdotal, but clearance has been noted as the patient ages. Although topical agents have been the mainstay of therapy, recent advancement in laser intervention for treatment of ulerythema ophryogenes is promising.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24605344

Source DB:  PubMed          Journal:  Cutis        ISSN: 0011-4162


  1 in total

1.  Ulerythema Ophryogenes in a Saudi Male: A Case Report.

Authors:  Nouf Algharbi; Yara Jazzar; Asem Shadid; Asem Almesfer
Journal:  Cureus       Date:  2022-07-05
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.