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Apr 24, 2024 · The International 22q11.2 Foundation is a nonprofit organization dedicated to supporting the needs of families and individuals affected by ...
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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 ...
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The major clinical manifestations of 22q11.2DS include congenital heart disease, particularly conotruncal malformations (ventricular septal defect, tetralogy of ...
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Jan 13, 2024 · This condition is due to missing part of chromosome 22. It may cause heart issues, thyroid problems, cleft palate, lower immunity and other ...
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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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2DS stands for 22q11.2 deletion syndrome. 22, Chromosome 22 (the smallest of the human chromosomes, in every cell of the body).
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