Literature DB >> 6467651

The Nance-Horan syndrome: a rare X-linked ocular-dental trait with expression in heterozygous females.

D Bixler, M Higgins, J Hartsfield.   

Abstract

This report describes two families with the Nance-Horan syndrome, an X-linked trait featuring lenticular cataracts and anomalies of tooth shape and number. Previous reports have described blindness in affected males but posterior sutural cataracts with normal vision as the primary ocular expression in heterozygous females. In one of these two families, the affected female is not only blind in one eye but reportedly had supernumerary central incisors (mesiodens) removed. This constitutes the most severe ocular and dental expression of this gene in heterozygous females yet reported.

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Year:  1984        PMID: 6467651     DOI: 10.1111/j.1399-0004.1984.tb00783.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  15 in total

1.  The Nance-Horan syndrome.

Authors:  I R Walpole; A Hockey; A Nicoll
Journal:  J Med Genet       Date:  1990-10       Impact factor: 6.318

2.  Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis.

Authors:  D Stambolian; R A Lewis; K Buetow; A Bond; R Nussbaum
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

3.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

4.  The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly.

Authors:  Manèl Chograni; Imen Rejeb; Lamia Ben Jemaa; Myriam Châabouni; Habiba Chaabouni Bouhamed
Journal:  Eur J Hum Genet       Date:  2011-05-11       Impact factor: 4.246

Review 5.  Molecular genetics of supernumerary tooth formation.

Authors:  Xiu-Ping Wang; Jiabing Fan
Journal:  Genesis       Date:  2011-04-01       Impact factor: 2.487

6.  A locus for isolated cataract on human Xp.

Authors:  P J Francis; V Berry; A J Hardcastle; E R Maher; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  2002-02       Impact factor: 6.318

7.  Ophthalmic pathology of Nance-Horan syndrome: case report and review of the literature.

Authors:  Xiaoyan Ding; Mrinali Patel; Alexandra A Herzlich; Pamela C Sieving; Chi-Chao Chan
Journal:  Ophthalmic Genet       Date:  2009-09       Impact factor: 1.803

8.  Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome.

Authors:  D Zhu; D M Alcorn; S E Antonarakis; L S Levin; P C Huang; T N Mitchell; A C Warren; I H Maumenee
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

9.  X-linked cataract and Nance-Horan syndrome are allelic disorders.

Authors:  Margherita Coccia; Simon P Brooks; Tom R Webb; Katja Christodoulou; Izabella O Wozniak; Victoria Murday; Martha Balicki; Harris A Yee; Teresia Wangensteen; Ruth Riise; Anand K Saggar; Soo-Mi Park; Naheed Kanuga; Peter J Francis; Eamonn R Maher; Anthony T Moore; Isabelle M Russell-Eggitt; Alison J Hardcastle
Journal:  Hum Mol Genet       Date:  2009-05-04       Impact factor: 6.150

10.  Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform.

Authors:  Shiwani Sharma; Kathryn P Burdon; Alpana Dave; Robyn V Jamieson; Yuval Yaron; Frank Billson; Lionel Van Maldergem; Birgit Lorenz; Jozef Gécz; Jamie E Craig
Journal:  Mol Vis       Date:  2008-10-20       Impact factor: 2.367

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