Bateman J B, Maumenee I H
Ophthalmic Paediatr Genet. 1984 Aug;4(2):59-66. doi: 10.3109/13816818409007839.
The ocular malformation of microcornea, uveal coloboma, high myopia, posterior staphyloma, and macrophthalmia was studied in a family. Clinical characteristics and ocular parameters, including refractive error and axial length, are summarized. The pedigree is consistent with autosomal dominant inheritance of the disorder; expressivity is variable. This unique malformation is differentiated from other well-recognized syndromes of colobomatous microphthalmia.
对一个家族中的小角膜、脉络膜缺损、高度近视、后巩膜葡萄肿和大眼球等眼部畸形进行了研究。总结了临床特征和眼部参数,包括屈光不正和眼轴长度。该家系符合该疾病的常染色体显性遗传;表现度可变。这种独特的畸形与其他公认的小眼裂缺损综合征不同。