PETERS ANOMALY - THE SPECTRUM OF ASSOCIATED OCULAR AND SYSTEMIC MALFORMATIONS

PETERS ANOMALY - THE SPECTRUM OF ASSOCIATED OCULAR AND SYSTEMIC MALFORMATIONS
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DOI:
10.3109/13816819209087614
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发表时间:
1992-06-01
期刊:
OPHTHALMIC PAEDIATRICS AND GENETICS
影响因子:
--
通讯作者:
MUSARELLA, MA
MUSARELLA, MA
中科院分区:
其他
文献类型:
--
作者:
HEON, E;BARSOUMHOMSY, M;MUSARELLA, MA

文献摘要

被引文献

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彼得斯异常的情况下,看到在过去的十年中,在医院圣贾斯汀在蒙特利尔,进行审查。在50%的病例中观察到相关的眼部异常,而60%的患者出现相关的全身缺陷。从这些患者和文献报道的患者中可以清楚地看出,Peters异常可能是一种孤立的疾病,也可能是不同综合征的一部分:Krause-Kivlin综合征或Peters+综合征。作者强调,如果要提供适当的管理,眼科医生认识到这些可能性的重要性。
The cases of Peters' anomaly seen over the past decade, at Hospital Ste-Justine in Montreal, are reviewed. Associated ocular anomalies were observed in 50% of cases while 60% of patients presented with associated systemic defects. It is clear, from these patients and those reported in the literature, that Peters' anomaly can be an isolated condition, or part of distinct syndromes: the Krause-Kivlin syndrome or the Peters'-plus syndrome. The authors emphasize the importance for the ophthalmologist to recognize these possibilities if proper management is to be provided.