Practical aspects of therapy for glutaric aciduria type 1

Practical aspects of therapy for glutaric aciduria type 1

Treatment of many of the diseases in the panel of expanded newborn screening includes dietary therapy. Glutaric aciduria type 1 (GA1) is a hereditary disorder caused by mutations in the gene GCDH, encoding glutaryl‑CoA dehydrogenase, an enzyme in the amino acid metabolic pathways. The decreased acti...

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Main Authors: E. Yu. Zakharova, S. V. Mikhailova, V. V. Zarubina, N. A. Krasnoshchekova, N. L. Pechatnikova, V. P. Vorontsova, D. I. Gribov, M. V. Zazivihina, А. N. Slatetskaya, M. V. Kurkina, P. V. Baranova, L. P. Nazarenko, S. А. Repina, L. R. Selimsyanova, N. D. Vashakmadse, T. V. Bushueva
Format: Article
Language:Russian
Published: ABV-press 2021-12-01
Series:Нервно-мышечные болезни
Subjects:
inherited metabolic diseases
glutaric aciduria type 1
diet therapy
specialized nutrition products
Online Access:https://nmb.abvpress.ru/jour/article/view/465
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