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L-2-hydroxyglutaric aciduria in two siblings.

László Sztriha·Aithala Gururaj·Peter Vreken·Michael Nork·Gilles Lestringant
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Abstract

Two Pakistani siblings with L-2-hydroxyglutaric aciduria are reported herein. A 6-year-old male and a 2-year-old female, born to consanguineous parents, had chronic slowly progressive neurodegenerative disorder with insidious onset after infancy. Mental regression and seizures were evident in both patients, whereas cerebellar dysfunction was the main motor handicap in the male and pyramidal symptoms were prominent in the female. Magnetic resonance imaging revealed bilateral symmetrical abnormal signal in the subcortical white matter, internal and external capsules, basal ganglia, and dentate nuclei. The underlying metabolic defect, which is likely inherited in an autosomal recessive mode, remains unknown in this disorder.

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Basal GangliaBrain Diseases, Metabolic, InbornChildChild, PreschoolDentate GyrusDevelopmental DisabilitiesFemaleGlutamatesHumansMagnetic Resonance ImagingMaleCase ReportsJournal Article

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László Sztriha, Aithala Gururaj, Peter Vreken, Michael Nork, Gilles Lestringant. 2002. L-2-hydroxyglutaric aciduria in two siblings.. https://doi.org/10.1016/s0887-8994(02)00405-8

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