Literature DB >> 432928

Phenotype i associated with congenital cataract in Japanese.

H Ogata, Y Okubo, T Akabane.   

Abstract

A Japanese family with two siblings of phenotype i is presented. Both had a past history of surgical treatment for congenital cataract. In Japan, 18 individuals of phenotype i, including our case, have been found in ten unrelated families. Seventeen of them had congenital cataract. Cataract was not found in any of the 45 phenotype I members in these families. It is briefly discussed why these two linked and quite rare genes were found in combination only in Japanese persons.

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Year:  1979        PMID: 432928     DOI: 10.1046/j.1537-2995.1979.19279160286.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  4 in total

1.  Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens, MIP (AQP0).

Authors:  P Francis; V Berry; S Bhattacharya; A Moore
Journal:  Br J Ophthalmol       Date:  2000-12       Impact factor: 4.638

2.  The genetics of cataract: our vision becomes clearer.

Authors:  J F Hejtmancik
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

Review 3.  The genetics of childhood cataract.

Authors:  P J Francis; V Berry; S S Bhattacharya; A T Moore
Journal:  J Med Genet       Date:  2000-07       Impact factor: 6.318

4.  Abnormalities caused by carbohydrate alterations in Ibeta6-N-acetylglucosaminyltransferase-deficient mice.

Authors:  Guo-Yun Chen; Hisako Muramatsu; Mineo Kondo; Nobuyuki Kurosawa; Yozo Miyake; Naoki Takeda; Takashi Muramatsu
Journal:  Mol Cell Biol       Date:  2005-09       Impact factor: 4.272

  4 in total

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