GLYCOSYLATION DISORDER SYNDROME TYPE 1b: DIAGNOSTICS AND TREATMENT

The article highlights the medical case of a rare hereditary disease — glycosylation disorder syndrome type 1b, unique for our country. This syndrome is referred to the heterogeneous group of the congenital diseases characterized by the disorder of glycoprotein synthesis as a result of the defects N...

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Bibliographic Details
Main Authors: Yu.S. Akoev, A.V. Migali, N.V. Zhurkova, O.B. Kondakova, E.A. Roslavtseva, A.R. Pinaeva, V.A. Skvortsova, I.I. Migali
Format: Article
Language:Russian
Published: Union of pediatricians of Russia 2008-09-01
Series:Педиатрическая фармакология
Online Access:https://www.pedpharma.ru/jour/article/view/765
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