Neonatal hereditary spherocytosis caused by a de novo frameshift mutation of the SPTB gene characterized by hydrops fetalis
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference10 articles.
1. Non-immune hydrops fetalis: a short review of etiology and pathophysiology;Bellini;Am J Med Genet A,2012
2. Outcomes and morbidities of patients who survive haemoglobin Bart's hydrops fetalis syndrome: 20-year retrospective review;Chan;Hong Kong Med J,2018
3. Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis;Hannah;Case Rep Womens Health,2017
4. The spectrum of SPTA1-associated hereditary spherocytosis;Chonat;Front Physiol,2019
5. Deficiency of alpha-spectrin synthesis in burst-forming units-erythroid in lethal hereditary spherocytosis;Whitfield;Blood,1991
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Severe Microcytic Anemia Caused by Complex Hereditary Spherocytosis and X-Linked Sideroblastic Anemia with Mutations in SPTB and ALAS2 Genes;Journal of Clinical Medicine;2023-03-02
2. Whole‐exome sequencing uncovered genetic diagnosis of severe inherited haemolytic anaemia: Correlation with clinical phenotypes;British Journal of Haematology;2022-07-12
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