Literature DB >> 3785879

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

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

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.

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Year:  1986        PMID: 3785879     DOI: 10.3109/13816818609076118

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  3 in total

1.  Oculocutaneous Albinism associated with Axenfeld's Anomaly: Three case reports.

Authors:  B R Keshav; Mahmood J Mohammed; Nasir Mahmood
Journal:  Sultan Qaboos Univ Med J       Date:  2010-04-17

2.  Clinical features of affected males with X linked ocular albinism.

Authors:  S J Charles; J S Green; J W Grant; J R Yates; A T Moore
Journal:  Br J Ophthalmol       Date:  1993-04       Impact factor: 4.638

3.  X linked ocular albinism in Japanese patients.

Authors:  T Shiono; M Tsunoda; Y Chida; M Nakazawa; M Tamai
Journal:  Br J Ophthalmol       Date:  1995-02       Impact factor: 4.638

  3 in total

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