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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 speech and language difficulties.
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22q11.2DS is an autosomal dominant contiguous gene deletion syndrome. In 22q11.2DS caused by a 3.0 (2.54)-Mb deletion, the deletion is de novo in ...
DiGeorge syndrome is caused by a problem called 22q11 deletion. This is where a small piece of genetic material is missing from a person's DNA. In about 9 in 10 ...
DiGeorge Syndrome (22q11.2 Deletion ... - Cleveland Clinic
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DiGeorge syndrome (22q11.2 deletion syndrome) is a genetic condition that affects several parts of your body. A missing piece of chromosome 22 causes it.
Jul 26, 2023 · Disease Overview. Summary. Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a disorder caused by a small piece of chromosome 22 missing.
Aug 3, 2022 · 22q11.2 deletion syndrome (DS 22q11.2) is a rare disease of genetic origin, caused by the loss of the q11.2 region of chromosome 22.