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3 e dysregulation that manifested as recurrent sinopulmonary, cutaneous, and mucosal infections and ref
4 ve genetic disorder that is characterized by sinopulmonary disease and reflects abnormal ciliary stru
5 a usually cause the chronic muco-obstructive sinopulmonary disease primary ciliary dyskinesia (PCD) a
7 e age 4 years later presented with recurrent sinopulmonary infection caused by organisms including St
8 also have susceptibility to candidiasis and sinopulmonary infection, as well as autoimmunity and squ
9 0 ligand (CD40L) deficiency causes recurrent sinopulmonary infection, Pneumocystis carinii pneumonia,
10 stigated the mechanisms underlying recurrent sinopulmonary infections and hypogammaglobulinemia in 15
12 ever, in the pediatric population, recurrent sinopulmonary infections early in life are common, which
13 tis, the presence of antinuclear antibodies, sinopulmonary infections, and common variable immunodefi
15 ficiency and dysregulation lead to recurrent sinopulmonary infections, herpes viremia, autoimmunity,
17 investigated the genetic basis of recurrent sinopulmonary infections, persistent EBV viremia, and EB
21 d primary immunodeficiency, causes recurrent sinopulmonary, Pneumocystis and Cryptosporidium species
22 considered in the differential diagnosis of sinopulmonary syndromes, bronchiolitis, and cryptic case
23 ive aspergillosis most commonly involves the sinopulmonary tract reflecting inhalation as the princip