Article
Novel Biallelic Variants in DLD Gene Cause a Reversible Sensory Neuropathy.
Clinical genetics - 1 Feb 2026
Wang Lu, Xiong Ying, Jiang Kaiyan, Tan Dandan, Zhang Liya, Zhu Min, Zhou Meihong, Qiu Yusen, Hong Daojun
Abstract excerpt
Dihydrolipoamide dehydrogenase deficiency (DLDD) is a rare autosomal recessive disorder that typically affects the liver, brain, and muscle. Peripheral neuropathy has not been previously associated with this condition. We report a novel case of DLDD in a 20-year-old woman who presented with recurrent hepatic dysfunction and progressive sensory neuropathy. Clinical evaluation, electrophysiology, and nerve biopsy...
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