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l-2 Hydroxyglutaric aciduria presenting with anxiety symptoms
l-2 Hydroxyglutaric aciduria is a rare autosomal recessively inherited metabolic disorder of organic acid metabolism. Cerebellar and pyramidal signs with progressive neurological syndromes, mental deterioration, tremors, seizures, epilepsy and rarely macrocephaly are clinical findings of the disease...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3702901/ https://ncbi.nlm.nih.gov/pubmed/23749824 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2013-009512 |
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