DiGeorge syndrome (DGS); Velocardiofacial syndrome (VCFS); Conotruncal anomaly face syndrome (CTAF); Opitz G/BBB syndrome; Cayler cardiofacial syndrome.
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What is 22q11 deletion syndrome also known as?
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The 22q11.2 deletion syndrome is a genetic disorder caused by a missing section (microdeletion) of chromosome 22, which is present from the time a child is ...
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22q11.2 Deletion syndrome or 22q (also referred to as Velocardiofacialsyndrome (VCFS), and/or DiGeorge syndrome) is a disorder caused by a small missing ...
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2 Deletion Syndrome is also known as VCFS, DiGeorge (DGS), Shprintzen Syndrome, CATCH 22, Conotruncal anomaly face syndrome and Cayler cardiofacial syndrome. .
22q11.2 deletion syndrome is a genetic condition that affects many parts of the body. It can cause intellectual disability, learning and social challenges, and ...
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Dec 1, 2019 · 22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by the deletion of a small piece ...
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22q11.2DS has also been known by many other names, including. DiGeorge syndrome, Shprintzen syndrome, and velocardiofacial syndrome (VCFS). Now that ...
DGS is one of several syndromes that has historically grouped under a bigger umbrella called 22q11 deletion syndromes, which include Shprintzen-Goldberg ...
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