Pagon R A
Surv Ophthalmol. 1981 Jan-Feb;25(4):223-36. doi: 10.1016/0039-6257(81)90092-8.
Ocular coloboma is common malformation which includes a spectrum of anomalies that ranges from iris coloboma to clinical anophthalmos. Coloboma is etiologically heterogeneous. As an isolated defect, it is usually inherited as an autosomal dominant disorder, although autosomal recessive inheritance also occurs. Patients with multiple malformations and coloboma may have a recognized malformation syndrome of unknown etiology, a single gene disorder, or chromosomal abnormality. Prognosis and recurrence risk can be determined only after complete evaluation of the patient and other family members.
眼裂缺损是一种常见的畸形,包括一系列异常情况,从虹膜缺损到临床上的无眼球症。眼裂缺损在病因上具有异质性。作为一种孤立的缺陷,它通常以常染色体显性遗传病的形式遗传,不过也会出现常染色体隐性遗传。患有多种畸形和眼裂缺损的患者可能患有病因不明的公认畸形综合征综合征、单基因疾病或染色体异常。只有在对患者及其他家庭成员进行全面评估后,才能确定预后和复发风险。