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.

Nephrotic syndrome

Nephrotic syndrome is a collection of findings resulting from glomerular dysfunction with an increase in glomerular capillary wall permeability associated with pronounced proteinuria. Nephrotic syndrome refers to the constellation of clinical findings that result from severe renal loss of protein, with Proteinuria and hypoalbuminemia, edema, and hyperlipidemia.


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(per page)
PMID (PMCID)
717924
FEMALE Infant
[Nephrotic syndrome and hereditary spherocytosis (author's transl)].
Gimenez Llort A, Camacho Diaz JA, Estella Aguado J, Garcia Garcia L.
An Esp Pediatr. 1978;11(8-9):629-32.
[Nephrotic syndrome and hereditary spherocytosis (author's transl)].