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2 deletion syndrome, is a syndrome caused by the deletion of a small segment of chromosome 22. The symptoms are caused by the lack of those genes. DiGeorge ...
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2 deletion syndrome commonly have congenital heart defects, in particular truncus arteriosus and tetralogy of Fallot, as well as facial abnormalities such as ...
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22q11.2 distal deletion syndrome is a rare genetic condition caused by a tiny missing part of one of the body's 46 chromosomes – chromosome 22.
Missing: q= 3A% 2Fen.
DiGeorge syndrome (DGS) is a congenital disorder with a broad phenotypic presentation, which results predominantly from the microdeletion of chromosome 22 at a ...
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DiGeorge syndrome (22q11.2 deletion syndrome) - Symptoms and causes
www.mayoclinic.org › syc-20353543
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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DiGeorge Syndrome (22q11.2 Deletion ... - Cleveland Clinic
my.clevelandclinic.org › health › diseases
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.
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