Congenital disorder of glycosylation - one size does not fit all: a parent's perspective.

Therapeutic advances in rare disease Pub Date : 2022-08-22 eCollection Date: 2022-01-01 DOI:10.1177/26330040221118099
Konstantin Feinberg
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Abstract

This article is written by the parent of a child living with PMM2-congenital disorder of glycosylation (abbreviated to PMM2-CDG). It provides a parental perspective of the journey taken from diagnosis to present day and details the effect of off-label treatment with epalrestat.

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先天性糖基化障碍-一刀切并不适合所有人:父母的观点。
本文由患有PMM2先天性糖基化障碍(简称PMM2-CDG)的儿童的父母撰写。它提供了从诊断到现在的父母视角,并详细介绍了依帕司他标签外治疗的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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