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2DS) can present with a wide range of features that are highly variable, even within families. The major clinical manifestations of 22q11.2DS include congenital ...
Missing: 3D% 253DX
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 ...
Missing: 3D% sa% 253DX
May 6, 2019 · Background: 22q11.2 deletion syndrome (22q11.2DS) is caused by recurrent, chromosome specific, low copy repeat mediated copy number losses ...
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22q 11.2 deletion syndrome (22q DS) is caused by a missing piece of genetic material on the long (q) arm of chromosome 22.
Missing: 3D% sa% 253DX
Dec 1, 2019 · The deletion occurs near the middle of the chromosome at a location designated q11.2. 22q11.2 deletion syndrome has many possible signs and ...
Missing: 3D% sa% 253DX
22q11.2 deletion syndrome shows a variable clinical phenotype that can range from mild to severe. Congenital heart defects (two-thirds of cases) include ...
Missing: 3D% sa% 253DX
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