Biallelic variants in two complex I genes cause abnormal splicing defects in probands with mild Leigh syndrome.

ABSTRACT: Leigh syndrome is a genetically heterogeneous disorder resulting from deficient oxidative energy biogenesis. The syndrome is characterized by subacute episodic decompensations, transiently elevated lactate, and necrotizing brain lesions most often in the striatum and brainstem. Acute decompensation is often triggered by viral infections. Sequalae from repeated episodes leads to progressive neurological deterioration and death. The severity of Leigh syndrome varies widely, from a rapid demise in childhood to rare adult presentations. Although the causes of Leigh syndrome include genes affecting a variety of different pathways, more than 75 of them are nuclear or mitochondrial encoded genes involved in the assembly and catalytic activity of mitochondrial respiratory complex I. Here we report

SUBMITTER: Johnstone T 

PROVIDER: S-EPMC7749052 | biostudies-literature | 2020 Sep - Oct

REPOSITORIES: biostudies-literature