Atypical Course of Hereditary Spherocytic Anemia With Severely Elevated Liver Enzymes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s13312-023-2867-1.pdf
Reference6 articles.
1. Güngör A, Yarali N, Fettah A, et al. Hereditary spherocytosis: retrospective evaluation of 65 children. Turk J Pediatr. 2018;60:264–9.
2. Rothman JA, Stevens JL, Gray FL, Kalfa TA. How I approach hereditary hemolytic anemia and splenectomy. Pediatr Blood Cancer. 2020;67:e28337.
3. Matsuura H, Shiraishi Y. Haemolytic crisis of hereditary spherocytosis. Postgrad Med J. 2022;98:68–9.
4. Qin L, Nie Y, Zhang H, et al. Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing. J Hum Genet. 2020;65:427–34.
5. Richmond CM, Campbell S, Foo HW, et al. Rapid identification of biallelic SPTB mutation in a neonate with severe congenital hemolytic anemia and liver failure. Mol Syndromol. 2020;11:50–5.
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1. Complications of Delayed Diagnosis and Challenges: Hereditary Spherocytosis with Hepatocellular Jaundice, a Case Report from Ethiopia;2023-09-20
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