Ginsberg J, Soukup S, Ballard E T
J Pediatr Ophthalmol Strabismus. 1982 Jul-Aug;19(4):37-41. doi: 10.3928/0191-3913-19820701-10.
A clinical and pathologic study of a neonate with mosaic trisomy 9 revealed findings similar to those in other cases with this chromosomal anomaly. Except for deeply-set eyes and small palpebral fissures with slight telecanthus, our ocular findings have not previously been described in mosaic trisomy 9. The most striking ocular pathologic alterations involved the anterior segment and included a keratolenticular adhesion and marked iris hypoplasia. There were similarities to Peters' anomaly as well as to ocular lesions associated with aplasia of th optic nerve and Lowe's and Potter's syndrome. The ocular and extraocular anomalies in our patient appear to have resulted from a mesodermal dysgenesis operational between one and five and a half months of gestation.
对一名患有9号染色体嵌合三体的新生儿进行的临床和病理研究显示,其结果与其他患有这种染色体异常的病例相似。除了深陷的眼睛、睑裂小且有轻度内眦距增宽外,我们的眼部检查结果此前在9号染色体嵌合三体中未曾有过描述。最显著的眼部病理改变累及眼前节,包括角膜晶状体粘连和明显的虹膜发育不全。与彼得斯异常以及与视神经发育不全、洛氏综合征和波特综合征相关的眼部病变存在相似之处。我们患者的眼内和眼外异常似乎是由妊娠1至5个半月期间发生的中胚层发育异常所致。