| Literature DB >> 26830532 |
J Park1,2, D-C Jeong3,4, J Yoo1,2, W Jang2,5, H Chae1,2, J Kim2, A Kwon2, H Choi2, J W Lee3, N-G Chung3, M Kim1,2, Y Kim1,2.
Abstract
The aim of this study was to describe the mutational characteristics in Korean hereditary spherocytosis (HS) patients. Relevant literatures including genetically confirmed cases with well-documented clinical summaries and relevant information were also reviewed to investigate the mutational gene- or domain-specific laboratory and clinical association. Twenty-five HS patients carried one heterozygous mutation of ANK1 (n = 13) or SPTB (n = 12) but not in SPTA1, SLC4A1, or EPB42. Deleterious mutations including frameshift, nonsense, and splice site mutations were identified in 91% (21/23), and non-hotspot mutations were dispersed across multiple exons. Genotype-phenotype correlation was clarified after combined analysis of the cases and the literature review; anemia was most severe in HS patients with mutations on the ANK1 spectrin-binding domain (p < 0.05), and SPTB mutations in HS patients spared the tetramerization domain in which mutations of hereditary elliptocytosis and pyropoikilocytosis are located. Splenectomy (17/75) was more frequent in ANK1 mutant HS (32%) than in HS with SPTB mutation (10%) (p = 0.028). Aplastic crisis occurred in 32.0% of the patients (8/25; 3 ANK1 and 5 SPTB), and parvovirus B19 was detected in 88%. The study clarifies ANK1 or SPTB mutational characteristics in HS Korean patients. The genetic association of laboratory and clinical aspects suggests comprehensive considerations for genetic-based management of HS.Entities:
Keywords: ANK1; SPTB; genotype-phenotype correlation; hereditary spherocytosis; molecular analysis
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Year: 2016 PMID: 26830532 DOI: 10.1111/cge.12749
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438