Results 151 to 160 of about 6,512 (195)
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Cholelithiasis and Spherocytosis in Peromyscus

Archives of Surgery, 1963
Gallstones have occurred in laboratory animals only after certain artificial conditions are met. Shortly after 1950, it was found that a colony of deer mouse (Peromyscus maniculatus) occasionally bore gallstones spontaneously.1This provided a unique opportunity to investigate gallstones occurring naturally in a suitable laboratory animal. A colony of 6,
W K, FITZPATRICK   +2 more
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Hereditary spherocytosis and hemochromatosis

Annals of Hematology, 2002
A 37-year-old male, splenectomized at the age of 1 year, was admitted to the ward with severe chest pain and signs of cardiogenic shock. Clinical investigations revealed the presence of both hemochromatosis and hereditary spherocytosis (HS). HLA typing showed A3,B7 and A24,B57 haplotypes and genetic analysis revealed homozygosity for the C282Y mutation.
Brandenberg JB   +3 more
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A Splenunculus in Hereditary Spherocytosis

British Journal of Haematology, 1968
Studies on a patient with hereditary spherocytosis and a functioning splenunculus are reported. An inverse relationship between splenic size and red cell survival was observed. Evidence was obtained which further verified that red cell survival in hereditary spherocytosis is not related to the shape or to the osmotic sensitivity of the cell and that ...
M P, Westerman, J L, Jenkins, K M, Bron
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Hereditary Spherocytosis And Polycythemia

Archives of Internal Medicine, 1965
POLYCYTHEMIA that was clinically indistinguishable from polycythemia vera was observed in a patient who had splenectomy to palliate the anemia and hemolysis of hereditary spherocytosis. Polycythemia occurred 14 years after splenectomy, and the rubrocytes retained the spherocytic shape.
T W, CLARK, R W, EWER
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Hereditary spherocytosis in the elderly

The American Journal of Medicine, 1988
Five patients with hereditary spherocytosis diagnosed in their seventh to ninth decades of life are presented. These patients are remarkable for absent or mild clinical manifestations of disease. Splenectomy is the recommended treatment for hereditary spherocytosis to avoid the complications of aplastic or hemolytic crisis.
E W, Friedman   +2 more
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HLA and Hereditary Spherocytosis

Vox Sanguinis, 1977
Abstract. The HLA types of two families with hereditary spherocytosis (HS) suggest that the HS gene(s) may be linked with the HLA locus. If substantiated by further family studies, this linkage would place HS on chromosome 6.; Accepted: February 14 ...
D P, Sengar   +3 more
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Hereditary Spherocytosis

NeoReviews, 2016
Neonatal jaundice is commonly encountered in the neonatal period. Although it is mostly asymptomatic, severe cases may present as encephalopathy or kernicterus. Hereditary spherocytosis (HS) is the most common cause of nonimmune hemolytic anemia and the third most common cause of kernicterus after glucose-6-phosphate-dehydrogenase deficiency and ABO ...
Vasudha Mahajan, Sunil K. Jain
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Hereditary Spherocytosis

2006
Abstract A 25-year-old Japanese man was admitted to the hospital because of fever, sore throat, and general malaise. He had been febrile for several days and had noticed that the color of his urine was unusually dark. On admission, his temperature was 37.8°C.
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Is spherocytosis inherited in hereditary spherocytosis?

1956
The question when and how the spherocyte originates in hereditary spherocytosis is still unsolved. According to Schartum-Hansen, Dameshek & Henstell the red cell precursor within the marrow and the reticulocyte just entering the blood are normal (not spherocytic).
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Hereditary Spherocytosis

Pediatrics in Review, 2004
Shafqat, Shah, Roger, Vega
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