新冠肺炎时代的溶酶体储存病:一例埃及α-葡萄糖苷病病例的报告和溶酶体储存病与COVID-19-19关系的总结。

Heba Saed El-Amawy, Heba Dawoud
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引用次数: 1

摘要

背景:我们报道了一例来自埃及的α-岩藻糖苷酶病,一种溶酶体储存障碍。该报告还包括对新冠肺炎与溶酶体储存疾病关系的简要回顾。病例介绍:一名18岁的女性患者,根据皮肤体征、特征相和全身症状被诊断为II型岩藻糖苷病,并通过基因分析确诊。该患者在新冠肺炎大流行期间死于新冠肺炎肺炎,此前她从父亲那里感染并住院治疗。结论:局部或全身免疫抑制的溶酶体储存性疾病患者可能易患新冠肺炎呼吸道并发症。应该对这些患者进行严格的护理和防护指南。
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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Lysosomal storage diseases in the era of COVID-19: a report of an Egyptian case of alpha-fucosidosis and a summary of the lysosomal storage diseases-COVID-19 relationship.

Background: We present a case of alpha-fucosidosis, a lysosomal storage disorder, from Egypt. The report also includes a brief review of the COVID-19 and lysosomal storage diseases relationship.

Case presentation: A female patient aged 18 years, diagnosed with type II fucosidosis, based on the cutaneous signs, characteristic facies, and systemic symptoms, and diagnosis was confirmed using genetic analysis. The patient died from COVID-19 pneumonia during the COVID-19 pandemic after getting the infection from her father and being hospitalized.

Conclusions: Patients with lysosomal storage diseases with local or systemic immune suppression may be predisposed to respiratory complications of COVID-19. Intense care with protective guidelines should be applied to those patients.

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