Ginat-Israeli T, Hurvitz H, Klar A, Blinder G, Branski D, Amir N
Department of Pediatrics, Bikur Cholim General Hospital, Jerusalem, Israel.
Neuropediatrics. 1993 Apr;24(2):103-6. doi: 10.1055/s-2008-1071523.
We report a 7-month-old female baby with recent onset of neurological manifestations and mucocutaneous candidiasis. Immunological findings were compatible with severe combined immune deficiency (SCID). Infectious etiology of the central nervous system (CNS) involvement was ruled out. Biotinidase deficiency was suspected because of the concomitance of neurological and immunological deficits and was confirmed by enzymatic assay. Comprehensive treatment, including bone marrow transplantation (BMT) and biotin, resulted in immunological recovery, but no improvement of neurological condition. Serial brain CT scans over a period of 2 1/2 years demonstrated profound progression of brain atrophy involving gray matter.
我们报告了一名7个月大的女婴,近期出现神经学表现和黏膜皮肤念珠菌病。免疫学检查结果符合严重联合免疫缺陷(SCID)。中枢神经系统(CNS)受累的感染性病因被排除。由于同时存在神经和免疫缺陷,怀疑为生物素酶缺乏,并通过酶学检测得以证实。包括骨髓移植(BMT)和生物素在内的综合治疗使免疫功能恢复,但神经状况未见改善。在2年半的时间里进行的系列脑部CT扫描显示,涉及灰质的脑萎缩有显著进展。