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先天性果糖代谢障碍中的糖基化次要异常。

Secondary disorders of glycosylation in inborn errors of fructose metabolism.

机构信息

Institut de Bioquímica Clínica, Servei de Bioquímica i Genètica Molecular, Hospital Clínic, Edificio Helios III, c/ Mejia Lequerica s/n, 08028, Barcelona, Spain.

出版信息

J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S273-8. doi: 10.1007/s10545-009-1219-4. Epub 2009 Sep 20.

Abstract

Adamowicz and colleagues raised the alert in 2007 about patients with atypical hereditary fructose intolerance (HFI) primarily misdiagnosed as CDG Ix. We describe a girl with neonatal hypertonia, facial trismus, absent swallowing and coughing reflexes, gastro-oesophageal reflux and sporadically elevated Krebs cycle metabolites and lactate. At 14 months microcephaly and hepatomegaly were noted, with hypertransaminasaemia but normal blood coagulation, glucose, phosphate, and absent urinary reducing substances. Neurological impairment persisted. Because of hepatic and neurological abnormalities with developmental delay, Tf IEF was performed and showed a severe type 1 pattern, resulting in a wrong diagnosis of CDG. Subsequently, an aversion to fruits suggested HFI, confirmed by the finding of ALDOB mutations (p.A150P/p.N335K). The girl improved with fructose-free diet, but liver cirrhosis led to hepatic transplantation. She is now 7 years old with good evolution; facial trismus and hypertonia reversed, but microcephaly persists. Transferrin MALDI-TOF MS characterization revealed underoccupation of glycosylation sites and glycan abnormalities, which reversed with dietary treatment. High maternal fructose concentrations might have caused neonatal abnormalities. Although in our patient's mother there is no fructose accumulation at present, it is possible that increased ingestion of fruits and vegetables during pregnancy, together with her heterozygosity, caused an accumulation of fructose that finally affected the fetus. We also describe slightly abnormal transferrin isoelectric focusing and MALDI-TOF MS patterns of intact transferrin and N-glycans in a fructose-1,6-bisphosphatase (FBP1)-deficient patient. While HFI is a well-known cause of secondary CDG, we found no reports of abnormal transferrin isoelectric focusing patterns in FBP1 deficiency and we introduce this condition as a possible secondary cause for altered transferrin isoelectric focusing.

摘要

阿道姆维奇及其同事于 2007 年对主要被误诊为 CDG Ix 的非典型遗传性果糖不耐受症(HFI)患者发出了警报。我们描述了一名患有新生儿期高张力、面部牙关紧闭、无吞咽和咳嗽反射、胃食管反流和周期性升高的克雷布斯循环代谢物和乳酸的女孩。14 个月时,发现了小头畸形和肝肿大,伴有高转氨酸血症但凝血、血糖、磷酸盐正常,且尿液中无还原物质。神经功能障碍持续存在。由于存在肝和神经异常以及发育迟缓,进行了 Tf IEF,结果显示严重的 1 型模式,导致 CDG 的错误诊断。随后,由于存在肝脏和神经异常以及发育迟缓,发现了对水果的厌恶,提示存在 HFI,并通过发现 ALDOB 突变(p.A150P/p.N335K)得到证实。女孩通过无果糖饮食得到改善,但肝硬化导致肝移植。现在她 7 岁,病情良好;面部牙关紧闭和高张力已逆转,但仍存在小头畸形。转铁蛋白 MALDI-TOF MS 特征显示糖基化位点和聚糖异常,饮食治疗后逆转。高母体果糖浓度可能导致新生儿异常。虽然目前患者母亲的果糖没有积累,但有可能是由于她在怀孕期间增加了水果和蔬菜的摄入,加上她的杂合性,导致果糖积累最终影响了胎儿。我们还描述了一个果糖 1,6-二磷酸酶(FBP1)缺乏症患者的转铁蛋白等电聚焦和 MALDI-TOF MS 模式的轻微异常,以及完整转铁蛋白和 N-聚糖。虽然 HFI 是继发性 CDG 的已知原因,但我们没有发现 FBP1 缺乏症中转铁蛋白等电聚焦模式异常的报道,我们将这种情况引入为转铁蛋白等电聚焦改变的可能继发性原因。

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