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Apr 24, 2024 · 2 Foundation is a nonprofit organization dedicated to supporting the needs of families and individuals affected by chromosome 22q11.2 ...
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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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Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are highly variable, even within families.
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22q11.2 Society is a UK registered charity supporting families affected by DiGeorge syndrome, VCFS and 22q11.2 deletion.
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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 ...
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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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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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