合計: 3 |
|
PMID (PMCID) | ||
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19953640 |
MALE | Infant |
Persistent jaundice in an infant with homozygous beta thalassemia due to co-inherited Crigler-Najjar syndrome. | ||
Aggarwal V, Seth A, Sharma S, Aneja S, Sammarco P, Fabiano C. Pediatr Blood Cancer. 2010;54(4):627-8. |
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Persistent jaundice in an infant with homozygous beta thalassemia due to co-inherited Crigler-Najjar syndrome. | ||
10532663 |
MIXED_SAMPLE | Child |
Tubulointerstitial renal failure in childhood leptospirosis. | ||
Vachvanichsanong P, Dissaneewate P, Mitarnun W. Pediatr Emerg Care. 1999;15(5):332-4. |
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Only one child, who had an underlying disease of beta-thalassemia/Hb E, had jaundice, hepatosplenomegaly, anemia, and thrombocytopenia. | ||
7367946 |
MALE | Child |
HbE-beta-thalassemia associated with G6PD deficiency. | ||
Carpentieri U, Haggard ME, Schneider RG, Hightower BJ. South Med J. 1980;73(4):518-20. |
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HbE, beta thalassemia, and G6PD deficiency were demonstrated in a 6-year-old Mexican-American child with anemia, jaundice, and delayed growth. |