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1 ut PS-exposed autophagic vesicles because of asplenia.
2 Q) in a child with both severe 46,XY-DSD and asplenia.
3 7.1 years and 64% had functional or anatomic asplenia.
4 ciency causes organ growth defects including asplenia.
5 eptibility to infection caused by functional asplenia.
6 e molecular determinants of human congenital asplenia.
7 t underlie spleen development and congenital asplenia, a condition linked to increased risk of overwh
8 ents with severe sepsis or septic shock with asplenia and 52 without asplenia were included.
9 s, we searched for patients with and without asplenia and community-acquired severe sepsis/septic sho
10 ctive lateralization including dextrocardia, asplenia and intestinal malrotation, suggesting that BCO
11                               A patient with asplenia and multiple red blood cell transfusions acquir
12 ng Diamond-Blackfan anemia (DBA), congenital asplenia and T cell leukemia.
13 or C3 deficiencies, 1 of isolated congenital asplenia, and 2 of Bruton disease (X-linked agammaglobul
14                          Although functional asplenia from infarctions may be a major contributor to
15                          Isolated congenital asplenia (ICA) is characterized by the absence of a sple
16 esis and the etiology of isolated congenital asplenia (ICA), a life-threatening human condition, are
17 spleen development, and Tlx1 deletion causes asplenia in mice.
18 n proposed in the pathogenesis of congenital asplenia in patients carrying mutations of the gene-enco
19 posplenism in older mice, recapitulating the asplenia of an HO-1-deficient patient.
20                                   Functional asplenia or hyposplenism may predispose patients to spon
21 % of OPSI patients vs 5% of patients without asplenia (P = .038).
22 quently in OPSI patients (42% vs 12% without asplenia; P < .001) and more frequently manifested as bl
23 ow overall (42% vs 8% among patients without asplenia; P < .001).
24 iary and organ laterality defects as well as asplenia, paralleling symptoms of the human condition ri
25 g chronic mucocutaneous candidiasis, AI, and asplenia, respectively, in 49 of 121 (40%) and 10 of 121
26 itulating the clinical symptoms of the human asplenia syndrome.
27                                              Asplenia was present in 76 patients (54%).
28         On multivariable Poisson regression, asplenia was the only predictive variable independently
29 or septic shock with asplenia and 52 without asplenia were included.
30 by a perinatal lethal skeletal dysplasia and asplenia, with severe malformation or absence of specifi

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