沃尔夫帕金森-怀特综合征的重叠代谢和内分泌功能障碍:原因还是结果?

P. Puthanveetil
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引用次数: 0

摘要

在北美和全球,十分之一的人患有孤儿/罕见疾病。在这些病人中,大部分是儿童,30%的儿童在头十年内死亡。根据国家罕见病组织数据库(NORD),大约有7000种罕见病(https://rarediseases.org)。这一观点肯定会阐明与罕见疾病共存的代谢和内分泌异常的重要性。一些罕见疾病已被证明伴有代谢异常,包括巴特氏综合征、辛德勒病、色素失禁、胱氨酸病、马凡病和沃尔夫帕金森怀特综合征。本文将重点讨论wpw综合征的心血管并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overlapping Metabolic and Endocrine Dysfunction during Wolff ParkinsonWhite Syndrome: A Cause or Consequence?
In North America and globally, 1 out of 10 people suffer from orphan/rare diseases. Among these patients which are mostly children, 30% of the children die within the first decade. According to National Organization for Rare Disease database (NORD), there are around approximately 7000 rare diseases (https://rarediseases.org). This view point would definitely shed light into the importance of metabolic and endocrine abnormalities that co-exist with a rare disease. Some of the rare diseases which have been shown to be accompanied by metabolic abnormalities include Bartter’s syndrome, Schindler disease, Incontinentia Pigmenti, Cystinosis, Marfan disease and Wolff Parkinson White syndrome. This article will specially focus on the cardiovascular complicationWPW syndrome.
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