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Showing results for q=https%3A%2F%2F22q.org%2f What-is-22q%2f Different-names-for-22q%2F
Different Names For 22q
  • DiGeorge syndrome (DGS)
  • Velocardiofacial syndrome (VCFS)
  • Conotruncal anomaly face syndrome (CTAF)
  • Opitz G/BBB syndrome.
  • Cayler cardiofacial syndrome.
People also ask
22q11.2 Deletion syndrome or 22q (also referred to as Velocardiofacialsyndrome (VCFS), and/or DiGeorge syndrome) is a disorder caused by a small missing ...
Missing: 3A% 2F22q.
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 conceived. The ...
Missing: 3A% 2F22q.
2 Deletion Syndrome is also known as VCFS, DiGeorge (DGS), Shprintzen Syndrome, CATCH 22, Conotruncal anomaly face syndrome and Cayler cardiofacial syndrome. ​.
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 ...
Missing: 3A% 2F22q.
2 deletion syndrome is a genetic condition that affects many parts of the body. It can cause intellectual disability, learning and social challenges, and speech ...
Missing: 3A% 2F22q.
2 deletion syndrome is called 22qDS or 22q for short. Older names for the same genetic difference include DiGeorge syndrome, velocardiofacial syndrome (VCFS), ...
Missing: https% 3A% 2F22q.
2DS is established by identification of a heterozygous deletion at chromosome 22q11.2 on chromosomal microarray analysis or other genomic analyses. Management.
Missing: 3A% 2F22q.
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