There are infantile, juvenile and adult forms of leukodystrophy. 脑白质病变分幼儿期、青少年期和成年期。
Neither paper indicated which form of leukodystrophy the men have there are about 40 known types of the largely genetic brain cell-damaging disorder or who diagnosed the brothers. 不管是媒体还是为兄弟俩诊断的人都没有指明他们患的是哪一类型的脑白质病变&可知的关于大脑细胞损伤性病变大约就有40种。
Matthew Clark, 39, of Lincoln, England and his brother Michael Clark, 42, last year were reportedly given a vague diagnosis of terminal leukodystrophy. 每日电讯报在去年报道称,39岁的马修·克拉克和他42岁的哥哥迈克尔·克拉克被初步诊断为脑白质病变晚期。
Progress about Diffusion-Tensor Imaging in detecting Children Leukodystrophy 应用弥散张量成像检查儿童脑白质的进展
Changes of brainstem auditory and somatosensory evoked potentials in late infantile form of metachromatic leukodystrophy and the diagnostic value. 晚婴型脑白质营养不良诱发电位改变及诊断价值探讨。
Leukodystrophy is not an independent disease, but a general name of a group of genetic diseases with myelination or maintains disorder which often happens in children. 脑白质营养不良并非一个独立的疾病,而是一组最常见于儿童的髓鞘形成或维持发生障碍的遗传性疾病的总称。
Clinical characteristics and diagnosis of metachromatic leukodystrophy in 10 cases 10例异染性脑白质营养不良的临床特征及其诊断
The clinical and experimental studies of metachromatic leukodystrophy 异染性脑白质营养不良的临床及实验室研究
Late-onset infantile metachromatic leukodystrophy without MRI abnormalities in white matter Study on Genotypes of Children with Beta-Thalassemia Major and Their Immune Abnormalities 无脑白质影像学改变的晚发婴儿型异染性脑白质营养不良重型珠蛋白生成障碍性贫血患儿基因突变及免疫紊乱的特点
We report the clinical neurological and pathological manifestations of a patient with metachromatic leukodystrophy. 报道1例少年型异染性脑白质营养不良的临床与病理。
Objective The clinical manifestation, electrophysiological, imaging and pathological characteristics and diagnosis of 3 patients with late-onset infantile metachromatic leukodystrophy without marked cranial MRI changes were analyzed and reviewed. 目的分析3例脑白质影像学无改变的晚发婴儿型异染性脑白质营养不良患儿的临床、电生理、影像学和病理学改变特点,总结其特征表现和诊断规律。
MRI appearance of metachromatic leukodystrophy in children 儿童异染性脑白质营养不良的MRI表现