Catalano R A, Nelson L B, Schaffer D B
Pediatric Ophthalmology Service of Wills Eye Hospital, Philadelphia, PA 19107.
Ophthalmic Paediatr Genet. 1988 Mar;9(1):5-6. doi: 10.3109/13816818809031473.
An infant with oculocutaneous albinism and congenital glaucoma is described. The association of these two uncommon congenital disorders might suggest a common defective factor. Theoretically this patient broadens the spectrum of disorders of neural crest cell migration associated with albinism.
本文描述了一名患有眼皮肤白化病和先天性青光眼的婴儿。这两种罕见先天性疾病的关联可能提示存在一个共同的缺陷因素。从理论上讲，该患者拓宽了与白化病相关的神经嵴细胞迁移障碍的疾病谱。
