机构:Karolinska Univ Hosp, Karolinska Inst, Novum, Dept Med Nutr, SE-14186 Stockholm, Sweden
Esteitie, N
Larsson, NG
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机构:
Karolinska Univ Hosp, Karolinska Inst, Novum, Dept Med Nutr, SE-14186 Stockholm, SwedenKarolinska Univ Hosp, Karolinska Inst, Novum, Dept Med Nutr, SE-14186 Stockholm, Sweden
Larsson, NG
[1
]
机构:
[1] Karolinska Univ Hosp, Karolinska Inst, Novum, Dept Med Nutr, SE-14186 Stockholm, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Novum, Dept Woman & Child Hlth, SE-14186 Stockholm, Sweden
encephalopathy;
cardiomyopathy;
mitochondria;
cytochrome c oxidase;
D O I:
10.1080/08035250410018256
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
A functional respiratory chain is dependent on protein components encoded by both mtDNA and nuclear DNA. Isolated cytochrome c oxidase (COX) deficiency is often caused by mutations in nuclear genes regulating the assembly of the 13 protein subunits of this complex. The accompanying paper by Zeman and co-workers reports that mutations in SCO2 are common in infantile COX deficiency and are associated with a very poor prognosis. Conclusion: Molecular diagnosis is often feasible in patients with COX deficiency and particular attention should be paid to mutations in COX assembly genes.