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Heart Disease In Velo-Cardio-Facial Syndrome (Svcf)

Author

Listed:
  • Alina- Costina LUCA

    (”Gr.T.Popa” University of Medicine and Pharmacy; Pediatric Cardiology, “Sfanta Maria” Emergency Clinical Hospital)

  • Anca Maria TICU

    (Pediatric Cardiology, “Sfanta Maria” Emergency Clinical Hospital)

  • Heidrun ADUMITRACHIOAIEI

    (Pediatric Cardiology, “Sfanta Maria” Emergency Clinical Hospital)

Abstract

Velo-cardio-facial syndrome or chromosome deletion 22q11.2, is the most common chromosomal microdeletia, estimated at approx. 1:4000 people. The syndrome is a heterogeneous entity that includes multiple birth defects: cardiac, facial, gastrointestinal, renal, thymic hypoplasia, palate abnormalities, variable cognitive retardation, behavioral phenotypes, and psychiatric disorders. Management involves a multidisciplinary approach by a team of specialists: geneticist, cardiologist, surgeon, neurologist, immunologist, endocrinologist, psychiatrist.

Suggested Citation

  • Alina- Costina LUCA & Anca Maria TICU & Heidrun ADUMITRACHIOAIEI, 2022. "Heart Disease In Velo-Cardio-Facial Syndrome (Svcf)," SEA - Practical Application of Science, Romanian Foundation for Business Intelligence, Editorial Department, issue 28, pages 33-36, May.
    • Handle: RePEc:cmj:seapas:y:2022:i:28:p:33-36
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