Le Fur J M, Le Meur F, Parent P, Toudic L, Castel Y
J Genet Hum. 1985 Dec;33(5):427-34.
Adrenoleucodystrophy (ALD) is an X-linked hereditary disease concerning very long chain fatty acid (VLCFA) metabolism. It affects cerebral white matter and adrenal cortex. In the adult form, (adrenomyeloneuropathy) we also find hypogonadism. The enzymatic anomaly, yet unknown, takes place in the peroxisome. The illness is diagnosed by plasma VLCFA amount determination. We actually have no efficient treatment. Prenatal diagnosis is possible, using both biochemical assays and linkage analysis to a DNA probe.
肾上腺脑白质营养不良(ALD)是一种与极长链脂肪酸(VLCFA)代谢相关的X连锁遗传病。它会影响脑白质和肾上腺皮质。在成人型(肾上腺脊髓神经病)中,还会出现性腺功能减退。这种酶异常发生在过氧化物酶体中,目前尚不清楚。该病通过测定血浆VLCFA含量来诊断。目前我们没有有效的治疗方法。利用生化检测和与DNA探针的连锁分析可以进行产前诊断。