Banerjee T K
Department of Neurology, National Neurosciences Center Calcutta, Peerless Hospital Campus, Garia, Kolkata, India.
Eur Rev Med Pharmacol Sci. 2004 Nov-Dec;8(6):275-81.
Fabry's disease is an X-linked recessive Lysosomal Storage disease. The underlying metabolic defect is deficiency of lysosomal enzyme ceramidetrihexosidase. The disease has multisystem involvement. Neurological manifestations include small-fiber polyneuropathy manifested as painful distal extremities and anhidrosis. Fabry's disease also presents with both small-vessel and cortical multiple cerebral infarcts. Enzyme-replacement therapy has been found effective but expensive. Gene therapy could evolve as the ultimate therapeutic strategy.
法布里病是一种X连锁隐性溶酶体贮积病。潜在的代谢缺陷是溶酶体酶神经酰胺三己糖苷酶缺乏。该疾病累及多系统。神经学表现包括小纤维多发性神经病,表现为远端肢体疼痛和无汗。法布里病还伴有小血管和皮质多发性脑梗死。已发现酶替代疗法有效但昂贵。基因治疗可能会发展成为最终的治疗策略。