Sidransky E, Sherer D M, Ginns E I
Clinical Neuroscience Branch, National Institute of Mental Health, Bethesda, Maryland 20892.
Pediatr Res. 1992 Oct;32(4):494-8. doi: 10.1203/00006450-199210000-00023.
A group of neonates with Gaucher disease with a particularly devastating clinical course is described. The phenotype of these infants is analogous to that of a Gaucher mouse, which was created by targeted disruption of the mouse glucocerebroside gene. Similar to the homozygous mutant mice with glucocerebrosidase deficiency, these infants present at or shortly after birth, have rapidly progressing fulminant disease, and many have associated ichthyotic skin and/or hydrops fetalis. This transgenetic mouse model of Gaucher disease has helped us to appreciate a distinct Gaucher phenotype. Potentially, as this technology is applied to create other animal models of metabolic diseases, it may enable the recognition of other, as yet unappreciated presentations of inherited disorders.
本文描述了一组患有戈谢病且临床病程特别严重的新生儿。这些婴儿的表型与通过靶向破坏小鼠葡萄糖脑苷脂基因而创建的戈谢病小鼠相似。与纯合子葡糖脑苷脂酶缺乏的突变小鼠类似,这些婴儿在出生时或出生后不久即出现,患有迅速进展的暴发性疾病,许多婴儿伴有鱼鳞病样皮肤和/或胎儿水肿。这种戈谢病转基因小鼠模型有助于我们认识到一种独特的戈谢病表型。随着这项技术有可能应用于创建其他代谢性疾病的动物模型,它可能有助于识别遗传性疾病的其他尚未被认识到的表现形式。