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原发性先天性青光眼合并胼胝体发育不全的罕见病例。

Rare Case Of Primary Congenital Glaucoma With Hypoplasia Corpus Callosum.

作者信息

Gunawan Prastiya Indra, Komaratih Evelyn, Etika Risa, Harianto Agus, Saharso Darto

机构信息

Division of Neurology, Department of Paediatrics.

Division of Glaucoma, Department of Ophthalmology.

出版信息

J Ayub Med Coll Abbottabad. 2018 Apr-Jun;30(2):286-288.

Abstract

UNLABELLED

Primary congenital glaucoma is a rare disease that causes elevated intraocular pressure within the first three years of life. Few studies have explored the association of primary congenital glaucoma with malformation of corpus callosum. We report on a six-month-old female presenting with unilateral primary congenital glaucoma associated with hypoplasia of corpus callosum in Indonesian infant. The patient had already undergone trabeculectomy surgery. However, there no obvious improvement following the procedure given the severity of the condition.

CONCLUSION

The failure rate of surgery in severe primary congenital glaucoma conditions is still very high, and therapy can usually preserve vision if early identification of mild or moderate form is made.

摘要

未标注

原发性先天性青光眼是一种罕见疾病,可在生命的头三年导致眼压升高。很少有研究探讨原发性先天性青光眼与胼胝体畸形之间的关联。我们报告了一名6个月大的印度尼西亚女婴,她患有单侧原发性先天性青光眼并伴有胼胝体发育不全。该患者已经接受了小梁切除术。然而,鉴于病情严重程度,术后没有明显改善。

结论

重度原发性先天性青光眼的手术失败率仍然很高,如果能早期识别轻度或中度形式,治疗通常可以保留视力。

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