Dyer Jon A, Winters Cleome J, Chamlin Sarah L
Division of Pediatric Dermatology, Children's Memorial Hospital, and Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60614, USA.
Pediatr Dermatol. 2005 Sep-Oct;22(5):457-60. doi: 10.1111/j.1525-1470.2005.00117.x.
The congenital disorders of glycosylation are a group of rare metabolic disorders with predominantly neurologic findings. Some variants of this disorder also exhibit cutaneous manifestations. We report a patient with a congenital disorder of glycosylation type Ia, the most common form, with emphasis on the cutaneous findings of this type, and summarize the cutaneous findings in the other forms of the disorder.
糖基化先天性疾病是一组以神经学表现为主的罕见代谢性疾病。该疾病的一些变体也有皮肤表现。我们报告一例Ia型糖基化先天性疾病患者,这是最常见的类型,重点介绍该型的皮肤表现,并总结该疾病其他类型的皮肤表现。