Yakinci C, Soylu H, Kutlu N O, Sener R N
Inönü University, Turgut Ozal Medical Center, Department of Pediatrics, Malatya, Turkey.
Comput Med Imaging Graph. 1999 May-Jun;23(3):169-72. doi: 10.1016/s0895-6111(99)00007-5.
Infantile-onset leukoencephalopathy of van der Knaap type is manifested by initially normal or near normal neurological findings despite infantile-onset megalencephaly and magnetic resonance imaging evidence of severe white matter affection. Until this entity was recently described, these cases were usually presented under the heading of atypical variants of Alexander disease. To date 63 individuals have been reported in English literature. We report a four-year-old boy presented in the first months of life with progressive megalencephaly, delay in walking, clumsiness, convulsions and magnetic resonance imaging evidence of diffuse swelling of white matter, cystic cavitations in frontal, temporal and parietal lobes.
范德·克纳普型婴儿期起病的白质脑病,其表现为尽管有婴儿期起病的巨头畸形以及磁共振成像显示严重的白质病变,但最初神经学检查结果正常或接近正常。在这个疾病实体最近被描述之前,这些病例通常被归类为亚历山大病的非典型变异型。迄今为止,英文文献中已报道了63例。我们报告了一名4岁男孩,在出生后的头几个月出现进行性巨头畸形、行走延迟、动作笨拙、惊厥,磁共振成像显示白质弥漫性肿胀,额叶、颞叶和顶叶有囊性空洞。