Gort Laura, Coll M Josep, Chabás Amparo
Institut de Bioquímica Clínica, Hospital Clínic, C/ Mejía Lequerica s/n, Edifici Helios III, 08028 Barcelona, Spain.
Mol Genet Metab. 2007 Sep-Oct;92(1-2):183-7. doi: 10.1016/j.ymgme.2007.05.011. Epub 2007 Jul 5.
Glycogen storage disease type II is an autosomal recessive disorder of glycogen metabolism due to deficiency of lysosomal acid alpha-glucosidase. We present the molecular and enzymatic analyses of 22 Spanish GSD II patients. Molecular analyses revealed nine novel mutations. The most common defects were mutations c.-32-13T>G (25%) and c.1076-1G>C (14%) and we report the first homozygous patient for c.1076-1G>C mutation presenting with an infantile form. Alleles bearing mutation c.-32-13T>G are associated with the same haplotype.
II型糖原贮积病是一种常染色体隐性糖原代谢紊乱疾病,由溶酶体酸性α-葡萄糖苷酶缺乏所致。我们对22例西班牙II型糖原贮积病患者进行了分子和酶学分析。分子分析发现了9种新的突变。最常见的缺陷是c.-32-13T>G(25%)和c.1076-1G>C(14%)突变,我们报告了首例携带c.1076-1G>C突变的纯合子患者,其表现为婴儿型。携带c.-32-13T>G突变的等位基因与相同的单倍型相关。