Kaur Parminder, Chaudhry Chakshu, Panigrahi Inusha, Srivastava Priyanka, Kaur Anupriya
Genetic Metabolic Unit, Department of Pediatrics, Advanced Pediatrics Centre, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Lab Med. 2022 May 5;53(3):e59-e61. doi: 10.1093/labmed/lmab084.
Glutathione synthetase (GSS) deficiency is a rare disorder, occurring with a frequency of less than 1 in 100,000 individuals worldwide. The clinical presentation may vary from mild to severe, and manifestations include hemolytic anemia, hyperbilirubinemia, metabolic acidosis, neurological problems, and sepsis. Herein, we present a case of a newborn boy with the most severe phenotype of GSS deficiency, diagnosed based on clinical features and increased urinary 5-oxoproline levels determined via gas chromatography mass spectrometry (GCMS) testing.
谷胱甘肽合成酶(GSS)缺乏症是一种罕见疾病,在全球范围内发病率低于十万分之一。临床表现可能从轻度到重度不等,症状包括溶血性贫血、高胆红素血症、代谢性酸中毒、神经问题和败血症。在此,我们报告一例患有最严重GSS缺乏症表型的男婴病例,该病例根据临床特征及通过气相色谱 - 质谱联用(GCMS)检测确定的尿中5 - 氧脯氨酸水平升高而确诊。