DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22. While the symptoms...
49 KB (5,271 words) - 23:49, 7 July 2024
Neural crest (section DiGeorge syndrome)
conditions such as frontonasal dysplasia, Waardenburg–Shah syndrome, and DiGeorge syndrome. Therefore, defining the mechanisms of neural crest development...
41 KB (4,587 words) - 04:18, 22 July 2024
Williams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. Facial features frequently include...
52 KB (5,772 words) - 04:08, 9 August 2024
LZTR1 (section DiGeorge Syndrome)
uncontrollably. DiGeorge syndrome (known as 22q11.2 deletion) caused by a deletion in the 22nd chromosome. Some of the typical symptoms associated with DiGeorge Syndrome...
9 KB (1,252 words) - 16:33, 22 November 2023
syndrome Turner syndrome Noonan syndrome Patau syndrome DiGeorge syndrome Cri du chat syndrome Edwards syndrome Fragile X syndrome Okamoto syndrome It...
4 KB (283 words) - 00:15, 31 January 2023
The microprocessor complex subunit DGCR8 (DiGeorge syndrome critical region 8) is a protein that in humans is encoded by the DGCR8 gene. In other animals...
6 KB (744 words) - 12:45, 5 April 2024
immunodeficiency now commonly referred to as DiGeorge syndrome. DiGeorge was the son of two Italian immigrants, Antonio DiGiorgio and his wife Emilia (née Taraborelli)...
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Klinefelter's syndrome Ovaries in Fanconi anemia, gonadal dysgenesis, trisomy X Thymus in DiGeorge syndrome Labia majora in popliteal pterygium syndrome Corpus...
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deletion syndromes are detectable using karyotyping techniques. DiGeorge syndrome or velocardiofacial syndrome – most common microdeletion syndrome Prader–Willi...
9 KB (930 words) - 05:41, 11 September 2023
DNA-Ligase IV, common gamma chain, WHN-FOXN1, ZAP-70 and complete DiGeorge syndrome. It is fatal without treatment. The symptoms are very similar to graft-versus-host...
5 KB (515 words) - 14:37, 27 October 2023