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

Mary Ella M Pierpont1, Pilar L Magoulas2, Saleh Adi3

  • 1Division of Genetics and Metabolism, Department of Pediatrics and Ophthalmology, and Children's Hospitals and Clinics of Minnesota, Saint Paul, Minnesota; pierp001@umn.edu.

Pediatrics
|September 3, 2014
PubMed

Insights

Cardio-facio-cutaneous (CFC) syndrome, a RASopathy, shares features with Noonan and Costello syndromes. This consensus conference established clinical management guidelines for accurate diagnosis and comprehensive care of CFC patients.

Area of Science:

  • Genetics and Molecular Biology
  • Pediatrics
  • Clinical Medicine

Background:

  • Cardio-facio-cutaneous (CFC) syndrome is a rare genetic disorder.
  • It is part of the RASopathy group, sharing features with Noonan and Costello syndromes.
  • CFC syndrome is characterized by craniofacial abnormalities, heart defects, skin issues, growth delays, and intellectual disability.

Purpose of the Study:

  • To establish clinical management guidelines for Cardio-facio-cutaneous syndrome.
  • To improve the diagnosis and care of individuals with CFC syndrome.
  • To provide a resource for healthcare professionals managing CFC syndrome.

Main Methods:

  • A consensus conference was organized by CFC International.
  • Experts from various medical specialties participated.
  • Clinical management guidelines were developed based on expert consensus.

Main Results:

  • The conference provided comprehensive clinical management guidelines for CFC syndrome.
  • These guidelines aim to assist in accurate diagnosis and best practice recommendations.
  • The guidelines facilitate long-term medical care for affected individuals.

Conclusions:

  • Accurate diagnosis and multidisciplinary care are crucial for managing CFC syndrome.
  • The developed guidelines will support healthcare providers in managing CFC patients.
  • These guidelines are essential for improving outcomes and support for individuals with CFC syndrome.

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