Combination of Osteogenesis imperfecta, Ehlers Danlos syndrome, TRAPsyndrome, and Stickler syndrome as multiple inherited connective tissue disordersin a 28-year-old Egyptian woman.

Hany El-Saadany, S. Negm
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引用次数: 1

Abstract

Collagen related diseases most commonly arise from genetic defects or nutritional deficiencies that affect the biosynthesis assembly posttranslational modification a secretion or other processes involved in normal collagen production. One thousand mutations have been identified in twelve out of more than twenty types of collagen. These mutations can lead to various diseases at the tissue level. This report describes an Egyptian female presented by multiple different polysystematic disorders proved to be manifestations of multiple rare inherited connective tissue disorders in the same patient to be the first woman worldwide to comprise all these rare syndromes up to our review.
成骨不全、Ehlers Danlos综合征、trap综合征和Stickler综合征合并为一名28岁的埃及女性的多重遗传性结缔组织疾病。
胶原蛋白相关疾病最常见的原因是遗传缺陷或营养缺乏,影响了生物合成组装、翻译后修饰、分泌或正常胶原蛋白产生的其他过程。在20多种胶原蛋白中,有12种已经发现了1000个突变。这些突变可以在组织水平上导致各种疾病。本报告描述了一名埃及女性,其表现为多种不同的多系统疾病,经证实为同一患者的多种罕见遗传性结缔组织疾病的表现,是世界上第一个包括所有这些罕见综合征的女性。
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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