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Arch Neurol. 2005 Apr;62(4):659-61.

Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene.

Author information

  • 1Centro de Investigación, Hospital Universitario 12 de Octubre, Madrid, Spain.

Abstract

BACKGROUND:

Mutations in the nuclear-encoded subunits of complex I of the mitochondrial respiratory chain are a recognized cause of Leigh syndrome (LS). Recently, 6 mutations in the NDUFS1 gene were identified in 3 families.

OBJECTIVE:

To describe a Spanish family with LS, complex I deficiency in muscle, and a novel mutation in the NDUFS1 gene.

DESIGN:

Using molecular genetic approaches, we identified the underlying molecular defect in a patient with LS with a complex I defect.

PATIENT:

The proband was a child who displayed the clinical features of LS.

RESULTS:

Muscle biochemistry results showed a complex I defect of the mitochondrial respiratory chain. Sequencing analysis of the mitochondrial DNA-encoded ND genes, the nuclear DNA-encoded NDUFV1, NDUFS1, NDUFS2, NDUFS4, NDUFS6, NDUFS7, NDUFS8, and NDUFAB1 genes, and the complex I assembly factor CIA30 gene revealed a novel homozygous L231V mutation (c.691C-->G) in the NDUFS1 gene. The parents were heterozygous carriers of the L231V mutation.

CONCLUSIONS:

Identifying nuclear mutations as a cause of respiratory chain disorders will enhance the possibility of prenatal diagnosis and help us understand how molecular defects can lead to complex I deficiency.

PMID:
15824269
[PubMed - indexed for MEDLINE]
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