Wanders R J, Schutgens R B, Barth P G, Tager J M, van den Bosch H
Department of Clinical Biochemistry, University Hospital Amsterdam, Netherlands.
Biochimie. 1993;75(3-4):269-79. doi: 10.1016/0300-9084(93)90087-9.
In recent years an increasing number of inherited decreases in man has been identified in which there is an impairment of one or more peroxisomal functions. Sofar 15 different peroxisomal disorders have been identified which can be subdivided into three distinct groups depending upon whether there is a generalized (group A), multiple (group B) or single (group C) loss of peroxisomal functions. In this paper we will briefly describe the functions of peroxisomes in man which are of direct relevance for the peroxisomal disorders known up to now. Based upon the biochemical characteristics of the different peroxisomal disorders, we well describe a straightforward approach for the postnatal identification of patients suspected to suffer from a peroxisomal disorder. Furthermore, a detailed analysis of the biochemical procedures which should be used preferably, is given.
近年来,人们已经发现越来越多的人类遗传性功能减退病例,其中一种或多种过氧化物酶体功能受到损害。到目前为止,已经确定了15种不同的过氧化物酶体疾病,根据过氧化物酶体功能是普遍丧失(A组)、多种丧失(B组)还是单一丧失(C组),可将这些疾病分为三个不同的组。在本文中,我们将简要描述过氧化物酶体在人类中的功能,这些功能与目前已知的过氧化物酶体疾病直接相关。基于不同过氧化物酶体疾病的生化特征,我们将描述一种直接的方法,用于出生后对疑似患有过氧化物酶体疾病的患者进行鉴定。此外,还对首选的生化检测方法进行了详细分析。