Departments of Orofacial Sciences and Pediatrics, and Institute of Human Genetics, University of California San Francisco, 513 Parnassus Ave., Box 0442, San Francisco, CA, 94143, USA,
Hepatol Int. 2008 Sep;2(3):390-4. doi: 10.1007/s12072-008-9078-x. Epub 2008 May 7.
Ornithine transcarbamylase (OTC) deficiency is an X-linked urea cycle defect. While hemizygous males typically present with hyperammonemic coma in infancy, reports of rare late-onset presentations exist, with poor outcomes in males up to 58 years old. Relatives with mutations identical to affected patients often remain asymptomatic, and it is likely that environmental and genetic factors influence disease penetrance and expression. Here, we present our investigation of a patient with late-onset presentation, and we emphasize the potential role of environmental and genetic factors on disease expression. The patient was a previously healthy 62-year-old man who developed mental slowing, refractory seizures, and coma over an 8-day period. Interestingly, the patient had recently used home gardening fertilizers and pesticides. Evaluations for drug and alcohol use, infections, and liver disease were negative. Despite aggressive therapy, blood NH(3) concentration peaked at 2,050 muM and the patient died from cerebral edema and cerebellar herniation. Analysis of the OTC gene showed a Pro-225-Thr (P225T) change in exon 7, a mutation that has been previously implicated in OTC deficiency. This case illustrates that OTC deficiency can cause acute, severe hyperammonemia in a previously healthy adult and that the P225T mutation can be associated with late-onset OTC deficiency. We speculate that exposure to organic chemicals might have contributed to the onset of symptoms in this patient. This case also emphasizes that persistent hyperammonemia may cause irreversible neurologic damage and that after the diagnosis of hyperammonemia is established in an acutely ill patient, certain diagnostic tests should be performed to differentiate between urea cycle disorders and other causes of hyperammonemic encephalopathy.
鸟氨酸氨甲酰基转移酶(OTC)缺乏症是一种 X 连锁尿素循环缺陷。虽然杂合子男性通常在婴儿期表现为高氨血症性昏迷,但也有罕见的迟发性病例报告,高达 58 岁的男性预后不良。与受影响患者突变完全相同的亲属通常无症状,并且环境和遗传因素可能影响疾病的外显率和表达。在这里,我们报告了一例迟发性病例的研究,并强调了环境和遗传因素对疾病表达的潜在作用。患者是一位 62 岁的健康男性,他在 8 天内出现精神迟钝、难治性癫痫发作和昏迷。有趣的是,患者最近使用了家庭园艺肥料和农药。药物和酒精使用、感染和肝病的评估均为阴性。尽管进行了积极的治疗,血液 NH(3)浓度峰值达到 2050 μM,患者死于脑水肿和小脑疝。OTC 基因分析显示第 7 外显子中存在 Pro-225-Thr(P225T)改变,该突变先前与 OTC 缺乏症有关。该病例说明 OTC 缺乏症可导致先前健康的成年患者发生急性、严重的高氨血症,并且 P225T 突变可与迟发性 OTC 缺乏症相关。我们推测暴露于有机化学物质可能导致了该患者症状的发作。该病例还强调,持续的高氨血症可能导致不可逆转的神经损伤,并且在急性病患者中确立高氨血症的诊断后,应进行某些诊断性检查以区分尿素循环障碍和其他高氨血症性脑病的原因。