Häberle Johannes, Görg Boris, Toutain Annick, Rutsch Frank, Benoist Jean-François, Gelot Antoinette, Suc Annie-Laure, Koch Hans Georg, Schliess Freimut, Häussinger Dieter
Klinik und Poliklinik für Kinder- und Jugendmedizin, Universitätsklinikum Münster, Albert-Schweitzer-Str. 33, 48129, Münster, Germany.
J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):352-8. doi: 10.1007/s10545-006-0256-5.
Glutamine synthetase (GS) is ubiquitously expressed in human tissues, being involved in ammonia detoxification and interorgan nitrogen flux. Inherited systemic deficiency of glutamine based on a defect of glutamine synthetase was recently described in two newborns with an early fatal course of disease. Glutamine was largely absent in their serum, urine and cerebrospinal fluid. Each of the patients had a homozygous mutation in the glutamine synthetase gene and enzymatic investigations confirmed that these mutations lead to a severely reduced glutamine synthetase activity. From the observation in the first patients with congenital glutamine synthetase deficiency, brain malformation can be expected as one of the leading signs. In addition, other organ systems are probably involved as observed in one of the index patients who suffered from severe enteropathy and necrolytic erythema of the skin. Deficiency of GS has to be added to the list of inherited metabolic disorders as a rare example of a defect in the biosynthesis of an amino acid.
谷氨酰胺合成酶(GS)在人体组织中广泛表达,参与氨的解毒和器官间的氮通量。最近在两名患有早期致命病程的新生儿中描述了基于谷氨酰胺合成酶缺陷的遗传性全身性谷氨酰胺缺乏症。他们的血清、尿液和脑脊液中基本没有谷氨酰胺。每个患者的谷氨酰胺合成酶基因都有纯合突变,酶学研究证实这些突变导致谷氨酰胺合成酶活性严重降低。从首例先天性谷氨酰胺合成酶缺乏症患者的观察结果来看,脑畸形有望成为主要体征之一。此外,正如其中一名患有严重肠病和皮肤坏死性红斑的索引患者所观察到的,其他器官系统可能也会受累。谷氨酰胺合成酶缺乏症作为氨基酸生物合成缺陷的罕见例子,必须被列入遗传性代谢紊乱列表中。