Medical Genetics Service, Hospital de Clínicas, Porto Alegre, RS, Brazil.
Am J Med Genet A. 2012 May;158A(5):1055-9. doi: 10.1002/ajmg.a.35271. Epub 2012 Apr 10.
Hunter disease or mucopolysaccharidosis type II (MPS II) is an X-linked recessive lysosomal disorder caused by the deficiency of iduronate-2-sulfatase, which is involved in the catabolism of the glycosaminoglycans (GAGs) heparan and dermatan sulphate. Our aim was to analyze three patients with severe Hunter syndrome that showed a total deletion of the iduronate-2-sulphatase (IDS) gene, after exon by exon PCR. DNA was used as a template for PCR synthesis of IDS, FRAXA, FRAXE, and DXS1113 specific amplicons. The DNA analysis for all three patients demonstrated a complete deletion of IDS, FRAXA, and FRAXE contiguous genes. We further performed SNP-array to delineate the deletion breakpoints and to characterize the deletion extension in the different patients. The results indicated a ∼9.4 Mb deletion in Patient 1, a ∼3.9 Mb deletion of the Xq27.3-Xq28 and a ∼3.1 Mb duplication of the X q28 region in Patient 2 and a ∼41.8 Kb deletion in Patient 3. SNP-array was shown to be important to map for deletion breakpoints. A comprehensive molecular analysis in patients with Hunter syndrome, especially in the ones presenting the severe form, is important to the understanding of the genetic determinants of the phenotype and for the genetic counseling to be provided to the families.
亨特病或黏多糖贮积症 II 型(MPS II)是一种 X 连锁隐性溶酶体贮积病,由艾杜糖-2-硫酸酯酶缺乏引起,该酶参与糖胺聚糖(GAGs)硫酸乙酰肝素和硫酸皮肤素的分解代谢。我们的目的是分析 3 名患有严重亨特综合征的患者,这些患者在 exon by exon PCR 后显示艾杜糖-2-硫酸酯酶(IDS)基因完全缺失。DNA 被用作 PCR 合成 IDS、FRAXA、FRAXE 和 DXS1113 特定扩增子的模板。对所有 3 名患者的 DNA 分析表明,IDS、FRAXA 和 FRAXE 连续基因完全缺失。我们进一步进行 SNP 芯片分析,以描绘缺失断点,并对不同患者的缺失扩展进行特征描述。结果表明,患者 1 存在约 9.4 Mb 的缺失,患者 2 存在约 3.9 Mb 的 Xq27.3-Xq28 缺失和约 3.1 Mb 的 Xq28 区域重复,患者 3 存在约 41.8 Kb 的缺失。SNP 芯片分析对于定位缺失断点非常重要。对亨特综合征患者进行全面的分子分析,特别是对表现出严重形式的患者进行分析,对于了解表型的遗传决定因素以及为患者家庭提供遗传咨询非常重要。