Cinaz P, Güvenir T, Gönlüşen G
Department of Pediatrics, Medical Faculty of Gazi University, Beşevler, Ankara, Turkey.
Acta Paediatr. 1993 Oct;82(10):892-3. doi: 10.1111/j.1651-2227.1993.tb17638.x.
Lipoid proteinosis (Urbach-Wiethe disease) is a rare autosomal recessive disorder in which hyalinized material is deposited in the skin, mucous membranes and brain. Laryngeal changes resulting in hoarseness may be present at birth or in early infancy, often being the first sign of the disease. A typical case is presented.
类脂蛋白沉积症(乌尔巴赫 - 维特病)是一种罕见的常染色体隐性疾病,其中透明样物质沉积于皮肤、黏膜和大脑。导致声音嘶哑的喉部改变可能在出生时或婴儿早期出现,常为该病的首发症状。现报道一典型病例。