Mayr Johannes A, Koch Johannes, Fauth Christine, Zimmermann Franz A, Rauscher Christian, Zschocke Johannes, Sperl Wolfgang
Department of Pediatrics, Paracelsus Medical University, Salzburg, Austria.
Neuropediatrics. 2012 Jun;43(3):130-4. doi: 10.1055/s-0032-1309308. Epub 2012 Apr 2.
Mutations in the X-linked E1α subunit of the pyruvate dehydrogenase complex (PHDC) are the most frequent causes of PDHC deficiency. The clinical picture is heterogeneous depending on residual enzyme activity and X-inactivation. We report on a girl who presented at an age of 3 weeks with muscular hypotonia, vomiting, hyperlactatemia, microcephaly, enlarged ventricles, partial agenesis of the corpus callosum, and seizures. PDHA1 sequencing was normal in DNA from blood. In muscle, normal PDHC activity was measured while substrate oxidation rates revealed moderately diminished pyruvate oxidation. Quantitative PCR analysis revealed hemizygosity of the whole PDHA1 gene. Homozygosity mapping and determination of the breakpoint showed a 1.1 million base pair deletion on the X-chromosome including the CDKL5 and PDHA1 genes. The difficulty in the diagnosis of PDHC deficiency is evident: (1) enzyme activity can be normal depending on the X-inactivation; (2) large deletions can be missed by routine genetic analysis; and (3) only quantification of the PDHA1 gene content revealed the mutation in our patient. We recommend to revisit patients who are clinically suspicious for a mitochondrial disorder especially for hidden PDHA1 mutations, such as large deletions.
丙酮酸脱氢酶复合体(PHDC)的X连锁E1α亚基突变是PHDC缺乏症最常见的病因。临床表现因残余酶活性和X染色体失活而异。我们报告了一名3周龄的女孩,她出现肌张力减退、呕吐、高乳酸血症、小头畸形、脑室扩大、胼胝体部分发育不全和癫痫发作。血液DNA中的PDHA1测序正常。在肌肉中,测量到正常的PHDC活性,而底物氧化率显示丙酮酸氧化略有降低。定量PCR分析显示整个PDHA1基因半合子。纯合子定位和断点测定显示X染色体上有110万个碱基对的缺失,包括CDKL5和PDHA1基因。PHDC缺乏症诊断的困难显而易见:(1)根据X染色体失活,酶活性可能正常;(2)常规基因分析可能遗漏大片段缺失;(3)只有对PDHA1基因含量进行定量才揭示了我们患者的突变。我们建议对临床上怀疑有线粒体疾病的患者进行复查,特别是对于隐藏的PDHA1突变,如大片段缺失。