Alqwaifly Mohammed, Bril Vera, Dodig Dubravka
College of Medicine, Qassim University, Buraydah, Saudi Arabia.
Ellen and Martin Prosserman Centre for Neuromuscular Diseases, Division of Neurology, Department of Medicine, University Health Network, University of Toronto, Toronto, Ontario, Canada.
Case Rep Neurol. 2019 Feb 8;11(1):32-36. doi: 10.1159/000496420. eCollection 2019 Jan-Apr.
The porphyrias are metabolic disorders due to a defect in the heme biosynthetic pathway. Patients have diverse clinical presentations with neuropathy being frequent in acute intermittent porphyria (AIP). Associated symptoms are abdominal pain and seizures. Three patients presenting with neuropathy were later diagnosed with AIP on the basis of clinical features, erythrocyte porphobilinogen deaminase activity, neuropathic patterns, and nerve conduction studies. Testing for the HMBS genetic mutation confirmed the diagnosis of AIP in 1 patient. The findings from this case series confirm that porphyric neuropathy in AIP is a predominantly motor neuropathy with differing neuropathic presentations ranging from focal motor neuropathy to quadriplegia and respiratory failure.
卟啉病是由于血红素生物合成途径缺陷引起的代谢紊乱。患者有多种临床表现,急性间歇性卟啉病(AIP)常伴有神经病变。相关症状为腹痛和癫痫发作。3例表现为神经病变的患者后来根据临床特征、红细胞卟胆原脱氨酶活性、神经病变模式和神经传导研究被诊断为AIP。对HMBS基因突变的检测在1例患者中确诊为AIP。该病例系列的研究结果证实,AIP中的卟啉性神经病变主要是运动性神经病变,其神经病变表现各异,从局灶性运动神经病变到四肢瘫痪和呼吸衰竭。