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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DiGeorge syndrome (22q11.2 deletion syndrome) - Symptoms and causes
www.mayoclinic.org › syc-20353543
Jan 13, 2024 · DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a condition caused when a small part of chromosome 22 is missing.
Dec 1, 2019 · is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location ...
Jul 26, 2023 · 2DS) is a disorder caused by a small piece of chromosome 22 missing. 22q11. ... The symptoms of this condition are extremely variable, even among ...
2DS is established by identification of a heterozygous deletion at chromosome 22q11.2 on chromosomal microarray analysis or other genomic analyses. Management.
22q11.2 deletion syndrome shows a variable clinical phenotype that can range from mild to severe. Congenital heart defects (two-thirds of cases) include ...
22q11.2 deletion syndrome is a genetic condition that causes a combination of medical problems. These problems can vary widely from child to child, ...
22q11.2 deletion syndrome is caused by a deletion of a small part of chromosome 22 near the middle of the chromosome at a location known as q11.2.
DiGeorge syndrome is a genetic condition caused by a missing piece of chromosome 22. Another name for DiGeorge syndrome is 22q11.2 deletion syndrome.
22q11.2 deletion syndrome is a genetic disorder that can cause many health problems. These problems may range from heart defects and developmental delays to ...
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