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About Velocardiofacial Syndrome Velocardiofacial syndrome is the most common syndrome associated with a cleft palate What is velocardiofacial syndrome? Velocardiofacial syndrome (VCFS) is a genetic condition that is sometimes hereditary VCFS is characterized by a combination of medical problems that vary from child to child
Velocardiofacial Syndrome (VCFS) - Developmental and Behavioral . . . In children with this syndrome, a tiny piece of one of the copies of chromosome 22 is missing This can cause many health problems These problems may range from heart defects and developmental delays to seizures The child may also have changes in how the eyes, nose, or ears look
Velocardiofacial - Conditions | UCSF Benioff Childrens Hospitals Velocardiofacial syndrome, or VCFS, is a complex syndrome that has been associated with more than 30 different characteristics, including defects of the palate, heart defects, learning disabilities and distinct facial features
About VCFS - Velo-Cardio-Facial Syndrome Educational Foundation’s (VCFS) Velo-cardio-facial syndrome is a genetic disorder with varying conditions present in each individual with the syndrome However, conditions that are common to the syndrome include certain heart defects, effects on facial appearance, and lack of or underdeveloped thymus and parathyroid glands
Velo-Cardio-Facial Syndrome - PMC Velocardiofacial syndrome (VCFS) also known as DiGeorge, conotruncal anomaly face and Cayler syndromes is caused by a microdeletion in the long arm of chromosome 22
Velo-Cardio-Facial Syndrome - Nicklaus Childrens Hospital Velo-cardio facial syndrome has a number of common features including a cleft palate, heart abnormalities, and a characteristic looking face, and many others What causes velo-cardio facial syndrome? While the exact cause is unknown, many children with VCFS have a missing portion of chromosome 22