I finally self diagnosed him, and narrowed it down to two syndromes: DiGeorge (which I would later find to be commonly called 22q) or Williams Syndrome. I ...
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Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Mar 23, 2023 · Their common genetic cause is a microdeletion (a very small piece of DNA is missing) from the long arm of chromosome 22. All of these conditions ...
Jun 7, 2019 · 2 deletion syndrome (22q11DS) is associated with behavioral and psychiatric complications such as schizophrenia (SCZ) autistic spectrum ...
Apr 24, 2024 · Grow. The International 22q11.2 Foundation is a nonprofit organization dedicated to supporting the needs of families and individuals affected by ...
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Disease summary: 22q11.2 deletion syndrome is a genetic defect, resulting in variable phenotypes including DiGeorge- or Shprintzen-syndrome.
We conclude that “modeling a model”, in this case 22q11DS as a model for idiopathic ASD, ADHD and SCZ, as well as other behavioral disorders like anxiety ...
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