L-2 hydroxyglutaric aciduria: report of a Mexican-Mayan patient with the mutation c.569C>T and response to vitamin supplements and levocarnitine-Reference-Cited by-同舟云学术

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L-2 hydroxyglutaric aciduria: report of a Mexican-Mayan patient with the mutation c.569C>T and response to vitamin supplements and levocarnitine

Published:2024 Issue:1 Volume:14 Page:
ISSN:2160-8288
Container-title:Tremor and Other Hyperkinetic Movements
language:en
Short-container-title:

Author:

Leal-Ortega Roberto^ORCID,Parra-Medina Luis Enrique^ORCID,González-Herrera Lizbeth Josefina^ORCID

Publisher

Ubiquity Press, Ltd.

Reference20 articles.

1. L-2-hydroxyglutaric aciduria –review of the literature and case series;Annals of Medicine and surgery,2023

2. A case report of chronic progressive pancerebellar syndrome with leukoencephalopathy: L-2 hydroxyglutaric aciduria;Movement Disorders Clinical Practice,2020

3. Progress in understanding 2-hydroxyglutaric acidurias;J Inherit Metab Dis,2012

4. Clinicoradiological spectrum of L-2-hydroxy glutaric aciduria: typical and atypical findings in an Indian Cohort;J Clin Imaging Sci,2019

5. L-2-hydroxyglutaric aciduria: a report of 29 patients;Turk J Pediatr,2005

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