Immunity, inflammation and disease · 2023
A new CECR1 mutation associated with severe hematological involvement in ADA2 deficiency.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
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Nicoară Delia, Niță Cristina, Stanilă Ana, Martiniuc Alexandru, Popa Laura, Petrescu Eliana, Bătăneant Mihaela, Ciofu Ruxandra, Guriță Adriana, Tabăcaru Radu, Ionescu Ruxandra, Groșeanu Laura
Аннотация
BACKGROUND: The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessively inherited disease resulting from loss-of-function mutations in ADA2, formerly named CECR1 (cat eye syndrome chromosome region, candidate 1) gene. Disease manifestations could be separated into three major phenotypes: inflammatory/vascular, immune dysregulatory, and hematologic; however, most patients presented with significant overlap between these three phenotype groups.
CASE PRESENTATION: We present a case of DADA2 deficiency with disease onset at 3 years old, not recognized till the age of 18 with severe gastrointestinal vasculitis and recurrent episodes of neutropenia associated with a new CECR1 mutation.
CASE PRESENTATION: We present a case of DADA2 deficiency with disease onset at 3 years old, not recognized till the age of 18 with severe gastrointestinal vasculitis and recurrent episodes of neutropenia associated with a new CECR1 mutation.