Beauregard S, Gilchrest B A
Dermatol Clin. 1987 Jan;5(1):109-21.
The classic premature aging syndromes are rare disorders, all of which clinically differ a great deal from the normal aging process. None is well understood at the biochemical level, and no specific treatment exists for any of these syndromes. Genetic counseling, preventive measures in some instances, and symptomatic treatment are available. The interest of gerontologists and geriatricians in these disorders derives in part from the expectation that such presumed single-gene mutations might contribute to our understanding of the molecular basis for normal aging. Unfortunately, to date, this expectation has not been realized.
经典的早衰综合征是罕见疾病,所有这些疾病在临床上与正常衰老过程有很大差异。在生化水平上,对它们都了解甚少,并且针对这些综合征中的任何一种都没有特效治疗方法。可提供遗传咨询、某些情况下的预防措施以及对症治疗。老年医学专家和老年病学家对这些疾病感兴趣,部分原因在于期望这类推测的单基因突变可能有助于我们理解正常衰老的分子基础。不幸的是,迄今为止,这一期望尚未实现。