Torres Vicente E, Harris Peter C, Pirson Yves
Mayo Clinic College of Medicine, Rochester, MN, USA.
Mayo Clinic College of Medicine, Rochester, MN, USA.
Lancet. 2007 Apr 14;369(9569):1287-1301. doi: 10.1016/S0140-6736(07)60601-1.
Autosomal dominant polycystic kidney disease is the most prevalent, potentially lethal, monogenic disorder. It is associated with large interfamilial and intrafamilial variability, which can be explained to a large extent by its genetic heterogeneity and modifier genes. An increased understanding of the disorder's underlying genetic, molecular, and cellular mechanisms and a better appreciation of its progression and systemic manifestations have laid out the foundation for the development of clinical trials and potentially effective treatments.
常染色体显性多囊肾病是最常见的、具有潜在致死性的单基因疾病。它存在较大的家族间和家族内变异性,这在很大程度上可由其遗传异质性和修饰基因来解释。对该疾病潜在的遗传、分子和细胞机制的深入理解,以及对其进展和全身表现的更好认识,为开展临床试验和研发潜在有效的治疗方法奠定了基础。