Attention deficit hyperactivity disorder: a rare clinical presentation of L-2-hydroxyglutaric aciduria

L-2-hydroxyglutaric aciduria (L2HGA) is a rare autosomal recessive neurometabolic disorder caused by the deficiency of L-2-hydroxyglutarate dehydrogenase (L2HGDH) enzyme. Dystonia, ataxia, pyramidal involvement and seizures are the common clinical manifestations. Coexisting behavioural problems and...

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Vydáno v:BMJ Case Rep
Hlavní autoři: George, Jithin, Sandhya, Pushpagiri, Sajitha, Kizhakethil Velliyatil, Sundaram, Soumya
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 2021
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8327819/
https://ncbi.nlm.nih.gov/pubmed/34330727
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2021-244038
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