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喘鸣作为核黄素反应性多种酰基辅酶A脱氢酶缺乏症的主要表现症状。

Stridor as the major presenting symptom in riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.

作者信息

Sperl W, Geiger R, Lehnert W, Rhead W

机构信息

Department of Paediatrics, University of Innsbruck, Austria.

出版信息

Eur J Pediatr. 1997 Oct;156(10):800-2. doi: 10.1007/s004310050717.

Abstract

UNLABELLED

Inspiratory stridor of unknown origin was the leading clinical symptom in an 11-month-old boy. The stridor increased over a period of 4 weeks, and assisted ventilation became necessary. Selective urinary screening by gas chromatography/mass spectrometry analysis revealed excretion of ethylmalonic and 3-OH-isovaleric acid and of N-isobutyryl-, N-2-methylbutyryl-, N-isovaleryl-, N-hexanoyl- and N-suberylglycine. Neither hypoglycaemia nor metabolic acidosis were noticed. Treatment with 200 mg of riboflavin per day led to a dramatic clinical improvement with restoration of normal respiration and an increase in muscular tone within 2 months. During this period, metabolite excretion in urine completely normalized. Riboflavin-sensitive multiple acyl-CoA dehydrogenation deficiency was confirmed in cultured fibroblasts. With riboflavin supplementation, the development of the child has been favourable, with normal school attendance now at an age of 9 years.

CONCLUSION

As respiratory symptoms might precede other symptoms in disorders of mitochondrial oxidation, we propose determination of urinary organic acids in all cases of unexplained laryngeal stridor.

摘要

未标注

一名11个月大的男童以不明原因的吸气性喘鸣为主要临床症状。喘鸣在4周内逐渐加重,最终需要辅助通气。通过气相色谱/质谱分析进行的选择性尿液筛查显示,尿中存在乙基丙二酸、3-羟基异戊酸以及N-异丁酰基、N-2-甲基丁酰基、N-异戊酰基、N-己酰基和N-辛二酰甘氨酸。未发现低血糖或代谢性酸中毒。每天给予200毫克核黄素治疗后,临床症状显著改善,2个月内呼吸恢复正常,肌张力增加。在此期间,尿中代谢物排泄完全恢复正常。在培养的成纤维细胞中证实存在核黄素敏感的多种酰基辅酶A脱氢酶缺乏症。补充核黄素后,该儿童发育良好,9岁时正常上学。

结论

由于在线粒体氧化障碍中呼吸症状可能先于其他症状出现,我们建议对所有不明原因的喉喘鸣病例进行尿有机酸测定。

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