Aliefendioğlu Didem, Tana Aslan A yşe, Coşkun Turgay, Dursun Ali, Cakmak Fatma Nur, Kesimer Mehmet
Social Security Children's Hospital, Neonatology Unit, Ankara, Turkey.
Pediatr Neurol. 2003 Feb;28(2):151-5. doi: 10.1016/s0887-8994(02)00501-5.
Transient nonketotic hyperglycinemia is characterized by clinical and biochemical findings similar to those seen in classic nonketotic hyperglycinemia. Abnormalities in amino acids are partially or completely resolved in a period ranging from days to months. Almost all patients with the classic form of nonketotic hyperglycinemia survive with severe neurologic sequela, whereas most of the patients with the transient form exhibit normal development. Therefore, distinguishing the transient form of nonketotic hyperglycinemia from classic nonketotic hyperglycinemia is important to predict outcome of the patients. Transient nonketotic hyperglycinemia has been reported in only seven neonates. This article adds two cases to the transient nonketotic hyperglycinemia and reviews the relevant literature. Common clinical features were determined, and presence of miotic pupils was stressed.
短暂性非酮症高甘氨酸血症的临床和生化表现与经典非酮症高甘氨酸血症相似。氨基酸异常在数天至数月的时间内部分或完全缓解。几乎所有经典型非酮症高甘氨酸血症患者存活下来都伴有严重的神经后遗症,而大多数短暂型患者发育正常。因此,区分短暂性非酮症高甘氨酸血症和经典非酮症高甘氨酸血症对于预测患者预后很重要。仅报道过7例新生儿患有短暂性非酮症高甘氨酸血症。本文新增2例短暂性非酮症高甘氨酸血症病例并复习相关文献。确定了常见的临床特征,并强调了瞳孔缩小的存在。