Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Mol Genet Metab. 2010 Dec;101(4):413-6. doi: 10.1016/j.ymgme.2010.08.008. Epub 2010 Aug 14.
We describe the outcome of two consecutive pregnancies with a clinical presentation of ornithine transcarbamylase (OTC) deficiency (OTCD) without a molecular diagnosis. A 119kb deletion on Xp11.4 including the OTC gene was detected in the mother. The same deletion was identified in the blood spots from deceased male newborns. In patients with a clinical and biochemical presentation of OTCD and negative OTC sequencing, whole genome or targeted chromosomal microarray analysis (CMA) with coverage of the OTC and neighboring genes should be performed as a reflex test.
我们描述了两例连续妊娠的结果,这些妊娠表现为精氨酰琥珀酸裂解酶(OTC)缺乏症(OTCD),但没有分子诊断。在母亲中检测到 Xp11.4 上包括 OTC 基因的 119kb 缺失。在死亡的男婴的血斑中也发现了相同的缺失。对于具有 OTCD 的临床和生化表现且 OTC 测序为阴性的患者,应作为反射试验进行全基因组或靶向染色体微阵列分析(CMA),以覆盖 OTC 和邻近基因。