合計: 2 |
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PMID (PMCID) | ||
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11318798 |
MIXED_SAMPLE | Infant |
Coinheritance of two alpha-spectrin gene defects in a recessive spherocytosis family. | ||
Dhermy D, Steen-Johnsen J, Bournier O, Hetet G, Cynober T, Tchernia G, Grandchamp B. Clin Lab Haematol. 2000;22(6):329-36. |
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We studied a recessive hereditary spherocytosis (HS) family from Norway in which all four children had haemolytic spherocytosis while spectrin (Sp) deficiency was detected in the proband. | ||
7967056 |
FEMALE | Middle Aged |
[Hereditary spherocytosis associated with non-Hodgkin's lymphoma in the spleen]. | ||
Arisawa K, Morita S, Kojima H, Inui A, Yoshino G, Hayashi Y, Kasuga M. Rinsho Ketsueki. 1994;35(9):871-5. |
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We diagnosed her hereditary spherocytosis (HS) from spherocytosis and family history and found a tumor in her enlarged spleen. |