Suppr超能文献

Nettleship-Falls X-linked ocular albinism with Axenfeld's anomaly. A case report.

作者信息

Hayakawa M, Kato K, Nakajima A, Yoshiike T, Ogawa H

出版信息

Ophthalmic Paediatr Genet. 1986 Aug;7(2):109-14. doi: 10.3109/13816818609076118.

Abstract

A Japanese male with Nettleship-Falls X-linked ocular albinism (NXOA) and associated with Axenfeld's anomaly is described here. The diagnosis of X-linked ocular albinism was difficult because of moderately pigmented fundus and lack of iris translucency, but macromelanosomes recognized by histological study of skin biopsy were helpful for diagnosis. This is the first report identifying the macromelanosomes in Japanese NXOA. A combination of ocular albinism and Axenfeld's anomaly is very rare. There might be a common defective factor for the development of these two congenital disorders.

摘要

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验