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Apr 24, 2024 · Info@22q.org. By Toll Free Phone 877-739-1849. By Mail International 22q11.2 Foundation, Inc. PO Box 532, Matawan, NJ 07747. Resources. For ...
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2 Deletion syndrome or 22q (also referred to as Velocardiofacialsyndrome (VCFS), and/or DiGeorge syndrome) is a disorder caused by a small missing piece of the ...
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Mar 23, 2023 · Their common genetic cause is a microdeletion (a very small piece of DNA is missing) from the long arm of chromosome 22. All of these conditions ...
The major clinical manifestations of 22q11.2DS include congenital heart disease, particularly conotruncal malformations (ventricular septal defect, tetralogy of ...
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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 ...
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Disease summary: 22q11.2 deletion syndrome is a genetic defect, resulting in variable phenotypes including DiGeorge- or Shprintzen-syndrome.
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