Warburg M
Division of Paediatric Ophthalmology and Handicaps, Gentofte Hospital, Denmark.
J Med Genet. 1993 Aug;30(8):664-9. doi: 10.1136/jmg.30.8.664.
A new classification of microphthalmos and coloboma is proposed to bring order to the complexity of clinical and aetiological heterogeneity of these conditions. A phenotypic classification is presented which may help the clinician to give a systematic description of the anomalies. The phenotype does not predict the aetiology but a systematic description of ocular and systemic anomalies improves syndrome identification. There are two major classes, total and partial microphthalmos, and a subclassification which follows the embryology of the anomalies. The aetiological classification consists of three classes: (1) genetic (monogenic and chromosomal), (2) prenatally acquired (teratological agents and intrauterine deformations), and (3) associations. Genetic disorders give rise to malformations; prenatally acquired anomalies are disruptions or deformations. The aetiological classification can be applied to other congenital birth defects and improves counselling of families. Recurrence risks vary considerably between the classes.
本文提出了一种小眼症和脉络膜缺损的新分类方法,旨在梳理这些病症临床和病因异质性的复杂性。文中给出了一种表型分类,这可能有助于临床医生对异常情况进行系统描述。该表型无法预测病因,但对眼部和全身异常情况进行系统描述有助于提高综合征的识别率。主要分为两大类,即完全性和部分性小眼症,并根据异常情况的胚胎学进行了细分。病因分类包括三类:(1)遗传性(单基因和染色体),(2)产前获得性(致畸因素和子宫内变形),以及(3)相关性。遗传性疾病会导致畸形;产前获得性异常则是破坏或变形。病因分类可应用于其他先天性出生缺陷,并改善对家庭的咨询。不同类别之间的复发风险差异很大。