Results 141 to 150 of about 1,234,995 (195)
Staphylococcus capitis Sepsis Complicated by Rapid Native Aortic Valve Endocarditis in Sickle Cell Disease: A Case Report. [PDF]
Patel RM, Sculthorpe TS, Abad A, Abad K.
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Further Support for Association of <i>DAND5</i> with Autosomal Recessive Laterality Disorders. [PDF]
Chorin O +15 more
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Sepsis Due to Capnocytophaga canimorsus Following a Fox Bite: A Case Report. [PDF]
Rahme C +4 more
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Association of Hiatus Hernia With Asplenia Syndrome
European Journal of Pediatrics, 1993During a 13-month period, 13 patients with asplenia syndrome were evaluated with MRI for cardiovascular and visceral anomalies. The MR images were reviewed for the presence of haitus hernia which was found in three patients. One of the remaining ten patients with no MRI evidence of hiatus hernia was diagnosed as having gastro-oesophageal reflux and ...
J K Wang, H C Lue, Chang M -H
exaly +3 more sources
Asplenia Syndrome With Atypical Cardiac Anomalies
Pediatric Cardiology, 1982Two infants with asplenia and complex cyanotic congenital heart disease showed unusual findings at cardiac catheterization. Each had a patent pulmonary outflow tract and a severe obstructive lesion of the aortic arch. These cases emphasize the heterogeneity of the asplenia-polysplenia syndromes. Pulmonary atresia or critical pulmonic stenosis is not an
Steven M Yabek, T Dillon, W Berman
exaly +3 more sources
Asplenia Syndrome in a Pair of Monozygotic Twins
Acta Paediatrica, International Journal of Paediatrics, 2006AbstractAsplenia syndrome is one of the heterotaxy syndromes, which many familial and animal studies suggest are caused by the loss of adequate genetic control of normal left–right asymmetry development. Moreover, there has not been any environmental factor documented to cause these syndromes.
Ju-Li Lin
exaly +3 more sources
ASPLENIA AND POLYSPLENIA SYNDROME
Acta Pathologica Japonica, 1982This report described the morphological characteristics of seven cases of asplenia syndrome and three of polysplenia syndrome. Each syndrome has been characterized by a tendency for symmetric development of normally asymmetric organs, with varying degrees of cardiovascular anomalies.
Y, Shinohara +12 more
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