Gorzelany Kerstin, Dursun Ali, Coşkun Turgay, Kalkanoğlu-Sivri Serap H, Gökçay Gülden Fatma, Demirkol Mübeccel, Feyen Oliver, Wendel Udo
Department of General Pediatrics, Heinrich-Heine University, Düsseldorf, Germany.
Turk J Pediatr. 2009 Mar-Apr;51(2):97-102.
In maple syrup urine disease (MSUD), disease-causing mutations can affect the BCKDHA, BCKDHB or DBT genes encoding for the E1alpha, E1beta and E2 subunits of the multienzyme branched-chain alpha-keto acid dehydrogenase (BCKDH) complex. Here we summarize the MSUD genotypes of a cohort of 32 unrelated Turkish patients in whom both alleles at a single gene locus harbored presumable disease-causing nucleotide changes. The patients had different forms of MSUD, ranging from the severe classical form (26 patients) to severe and mild variants (6 patients). In all except two patients (92%), the mutations occurred homozygously. The mutational spectrum included 27 different sequence variations--12 changes in the BCKDHA, 10 in the BCKDHB, and 5 in the DBT genes. In 37% (12 patients) of a total of 64 alleles, the supposed disease-causing mutations were located in the BCKDHA gene, in 44% (14 patients) in the BCKDHB gene and in 19% (6 patients) in the DBT gene. The mutational profile is heterogeneous, although two mutations occurred three times and five mutations occurred twice. There was no cluster for a single mutation except for c.773G>A (p.Cys258Tyr) in the BCKDHA gene, a hypothetical founder mutation in the Camlidere population.
在枫糖尿症(MSUD)中,致病突变可影响编码多酶支链α-酮酸脱氢酶(BCKDH)复合物E1α、E1β和E2亚基的BCKDHA、BCKDHB或DBT基因。在此,我们总结了一组32名无亲缘关系的土耳其患者的MSUD基因型,这些患者在单个基因位点的两个等位基因均携带可能致病的核苷酸变化。患者患有不同形式的MSUD,从严重的经典型(26例患者)到严重和轻度变异型(6例患者)。除两名患者外(92%),所有突变均为纯合子。突变谱包括27种不同的序列变异——BCKDHA基因中有12种变化,BCKDHB基因中有10种,DBT基因中有5种。在总共64个等位基因中,37%(12例患者)的假定致病突变位于BCKDHA基因,44%(14例患者)位于BCKDHB基因,19%(6例患者)位于DBT基因。突变谱是异质性的,尽管有两个突变出现了三次,五个突变出现了两次。除了BCKDHA基因中的c.773G>A(p.Cys258Tyr),这是Camlidere人群中的一个假定的奠基者突变外,没有单个突变的聚集现象。