Accumulation of ILC1 Cells in a DiGeorge Syndrome Patient withIntestinal Inflammation
2016
DiGeorge Syndrome (DGS) is a genetic disorder caused by a microdeletion of chromosome 22q11.2. Its classical features include congenital heart disease, abnormal facies, speech delay and hypocalcaemia [1]. The gastrointestinal complaints are also very common. However, the mechanisms of DGS with intestinal inflammation remain elusive.
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