Cardio-facio-cutaneous syndrome: Clinical features, diagnosis, and management guidelines

Mary E lla M Pierpont, Pilar L. Magoulas, Saleh Adi, Maria I nes Kavamura, Giovanni Neri, Jacqueline Noonan, Elizabeth I. Pierpont, Kent Reinker, Amy E. Roberts, Suma Shankar, Joseph Sullivan, Melinda Wolford, Brenda Conger, Molly Santa Cruz, Katherine A. Rauen

Research output: Contribution to journalReview articlepeer-review

71 Scopus citations

Abstract

Cardio-facio-cutaneous syndrome (CFC) is one of the RASopathies that bears many clinical features in common with the other syndromes in this group, most notably Noonan syndrome and Costello syndrome. CFC is genetically heterogeneous and caused by gene mutations in the Ras/mitogen-activated protein kinase pathway. The major features of CFC include characteristic craniofacial dysmorphology, congenital heart disease, dermatologic abnormalities, growth retardation, and intellectual disability. It is essential that this condition be differentiated from other RASopathies, as a correct diagnosis is important for appropriate medical management and determining recurrence risk. Children and adults with CFC require multidisciplinary care from specialists, and the need for comprehensive management has been apparent to families and health care professionals caring for affected individuals. To address this need, CFC International, a nonprofit family support organization that provides a forum for information, support, and facilitation of research in basic medical and social issues affecting individuals with CFC, organized a consensus conference. Experts in multiple medical specialties provided clinical management guidelines for pediatricians and other care providers. These guidelines will assist in an accurate diagnosis of individuals with CFC, provide best practice recommendations, and facilitate long-term medical care.

Original languageEnglish (US)
Pages (from-to)e1149-e1162
JournalPediatrics
Volume134
Issue number4
DOIs
StatePublished - 2014

Keywords

  • Braf mutation
  • Cardio-facio-cutaneous syndrome
  • Management guidelines
  • Mek1 mutation
  • Mek2 mutation
  • RASopathy

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