Results 21 to 30 of about 5,957 (204)
Background Isolated congenital asplenia (ICA) is a rare and life-threatening condition that predisposes patients to severe bacterial infections. Most of the reported cases are familial and the mode of inheritance is usually autosomal dominant.
Shigeo Iijima
doaj +2 more sources
Ivemark syndrome: asplenia with kidney collecting duct cysts and polysplenia with cerebellar cyst
Two newborns, one male and one female, from two different families, with Ivemark syndrome proven at autopsy are reported. One of them had asplenia and another had polysplenia.
V Krźelj +5 more
doaj +1 more source
Asplenia syndrome is frequently complicated by a total anomalous pulmonary venous connection. Pulmonary venous obstruction, following total anomalous pulmonary venous connection surgery, is one of the risk factors for morbidity and mortality.
Hideharu Oka +4 more
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Asplenia in a patient with Fanconi's anemia-like congenital aplastic anemia
Fanconi's anemia (FA) is an autosomal recessive disease manifested by pancytopenia resulting from bone marrow failure, variable physical anomalies and cancer susceptibility.
E Erduran, A Okten, G Kaya, A Yildiran
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Background Patients with asplenia have a significantly increased lifelong risk of severe invasive infections, particular post-splenectomy sepsis (PSS).
Marianne Bayrhuber +5 more
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Sickle cell disease (SCD) is caused by a point mutation in the beta-globin gene. SCD is characterized by chronic hemolytic anemia, vaso-occlusive events leading to tissue ischemia, and progressive organ failure.
Sari Peretz +11 more
doaj +1 more source
The spleen plays a dual role of immune response and the filtration of red blood cells (RBC), the latter function being performed within the unique microcirculatory architecture of the red pulp.
Lucie Dumas +7 more
doaj +1 more source
Background Asplenia vaccination is employed before ABO‐incompatible (ABOi) transplantation in case splenectomy is needed. Pneumococcal vaccines have been reported, in different patient groups, to increase anti‐A/B titers, through cross‐reactivity to ...
Elisa Bongetti +2 more
doaj +1 more source
ZEB2, a new candidate gene for asplenia. [PDF]
International audience: Primary asplenia is a rare condition with poorly known etiology. Mowat-Wilson syndrome (MWS) is characterized by typical facial dysmorphisms, intellectual disability, microcephaly, epilepsy and the possible presence of internal ...
Patrick Edery +9 more
core +1 more source
Splenectomy or congenital asplenia in humans increases susceptibility to infections. We have previously reported that congenital asplenia in zebrafish reduces resistance to Aeromonas hydrophila infection.
Lang Xie +8 more
doaj +1 more source

