VCF syndrome (medical condition): A genetic disorder which can present with a wide range of phenotypic manifestations which has lead to a number of different names being assigned to the various presentations e.g. DiGeorge Syndrome and Cayler Anomaly Face Syndrome. There are nearly 200 different symptoms that can occur and the severity of the condition is also highly variable depending on the nature and severity of the symptoms that are present.
See also:
Velocardiofacial syndrome:
»Introduction: Velocardiofacial syndrome
»Symptoms of Velocardiofacial syndrome
VCF syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that VCF syndrome, or a subtype of VCF syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
VCF syndrome: Another name for Velocardiofacial syndrome (or close medical condition association).
»Introduction: Velocardiofacial syndrome
»Symptoms of Velocardiofacial syndrome
VCF syndrome: VCF syndrome is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of VCF syndrome incude:
See full list of 188 symptoms of VCF syndrome (Velocardiofacial syndrome)
These medical disease topics may be related to VCF syndrome:
Source - NIH
Search to find out more about VCF syndrome:
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