Goker-Alpan Ozlem, Schiffmann Raphael, Park Joseph K, Stubblefield Barbara K, Tayebi Nahid, Sidransky Ellen
Section on Molecular Neurogenetics, NIMH/NIH, 49 Convent Drive, MSC 4405, Bethesda, MD 20892-4405, USA.
J Pediatr. 2003 Aug;143(2):273-6. doi: 10.1067/S0022-3476(03)00302-0.
Neuronopathic Gaucher disease, classically divided into two types, can have a continuum of phenotypes, often defying categorization. Nine children had an intermediate phenotype characterized by a delayed age of onset but rapidly progressive neurological disease, including refractory seizures and oculomotor abnormalities. There was genotypic heterogeneity among these patients.
经典地分为两种类型的神经元型戈谢病,其表型具有连续性,常常难以分类。九名儿童具有中间型表型,其特征为发病年龄延迟,但神经系统疾病进展迅速,包括难治性癫痫和动眼神经异常。这些患者存在基因异质性。