Hereditary spherocytosis

Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.

Thrombocytopenia

A reduction in the number of circulating thrombocytes.


Total: 2

                       


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PMID (PMCID)
1334393
 MIXED_SAMPLE Infant
[24 cases of human parvovirus B19 infection in children].
Borreda D, Palomera S, Gilbert B, Lienhardt A, de Lumley L.
Ann Pediatr (Paris). 1992;39(9):543-9.
Four patients had hematologic manifestations, including one case of transient bone marrow aplasia revealing hereditary spherocytosis, one case of autoimmune hemolytic anemia with beta-thalassemia, and two cases of peripheral thrombocytopenia.
3973056
 MIXED_SAMPLE Adult
Postsplenectomy sepsis 10 years or more after operation.
Evans DI.
J Clin Pathol. 1985;38(3):309-11.
The major predisposing illnesses were trauma, hereditary spherocytosis, and idiopathic thrombocytopenia.