Wehr H, Zaremba J
Zakładu Genetyki Instytutu Psychiatrii i Neurologii, Warszawie.
Neurol Neurochir Pol. 1991 Nov-Dec;25(6):769-74.
The properties and metabolic functions of peroxisomes are discussed. Classification and clinical symptoms of various diseases resulting from deficiencies of those organellae are presented. Most of the diseases involve the nervous system. The detection and determination of long-chain fatty acids (containing over 26 carbon atoms) is the principal diagnostic method in peroxisomal diseases.
本文讨论了过氧化物酶体的特性和代谢功能。介绍了因这些细胞器缺陷导致的各种疾病的分类和临床症状。大多数疾病累及神经系统。长链脂肪酸(含超过26个碳原子)的检测和测定是过氧化物酶体疾病的主要诊断方法。