Literature DB >> 19941417

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

Xiaoyan Ding1, Mrinali Patel, Alexandra A Herzlich, Pamela C Sieving, Chi-Chao Chan.   

Abstract

BACKGROUND: Nance-Horan syndrome (NHS) is a rare X-linked disorder typified by dense congenital central cataracts, microcornea, anteverted and simplex pinnae, brachymetacarpalia, and numerous dental anomalies due in most cases to a mutation in the NHS gene.
MATERIAL AND METHODS: We present a case of clinical manifestation and ocular pathology in a patient with NHS. This article also reviews and discusses the relevant literature.
RESULTS: Classic and novel ocular pathological findings of a young male with NHS are described, including congenital cataracts, infantile glaucoma, scleral staphyloma, and severe retinal cystoid degeneration.
CONCLUSIONS: We report a new pathological finding of severe retinal cystoid degeneration in this NHS patient and confirm abnormal development of the anterior chamber angle structure. These findings, coupled with our analysis of the available NHS literature, provide new understanding of the histopathological basis of ocular abnormalities and vision loss in NHS.

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Year:  2009        PMID: 19941417      PMCID: PMC2791400          DOI: 10.1080/13816810902822021

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  32 in total

1.  Severe visual impairment and retinal changes in a boy with a deletion of the gene for Nance-Horan syndrome.

Authors:  R Mathys; H Deconinck; K Keymolen; A Jansen; H Van Esch
Journal:  Bull Soc Belge Ophtalmol       Date:  2007

Review 2.  [Cataracts-oto-dental defects (Nance-Horan syndrome)].

Authors:  T Sonoda
Journal:  Ryoikibetsu Shokogun Shirizu       Date:  2001

3.  X-linked cataract.

Authors:  M Fraccaro; G Morone; U Manfredini; R Sanger
Journal:  Ann Hum Genet       Date:  1967-08       Impact factor: 1.670

Review 4.  Paediatric aphakic glaucoma.

Authors:  Caitriona Kirwan; Michael O'Keefe
Journal:  Acta Ophthalmol Scand       Date:  2006-12

5.  Organization and annotation of the Xcat critical region: elimination of seven positional candidate genes.

Authors:  Kristen M Huang; Scarlett Geunes-Boyer; Sufen Wu; Amalia Dutra; Jack Favor; Dwight Stambolian
Journal:  Genomics       Date:  2004-05       Impact factor: 5.736

6.  Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

Authors:  Kathryn P Burdon; James D McKay; Michèle M Sale; Isabelle M Russell-Eggitt; David A Mackey; M Gabriela Wirth; James E Elder; Alan Nicoll; Michael P Clarke; Liesel M FitzGerald; James M Stankovich; Marie A Shaw; Shiwani Sharma; Srecko Gajovic; Peter Gruss; Shelley Ross; Paul Thomas; Anne K Voss; Tim Thomas; Jozef Gécz; Jamie E Craig
Journal:  Am J Hum Genet       Date:  2003-10-16       Impact factor: 11.025

7.  Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance-Horan syndrome in the extended family.

Authors:  Adi Reches; Yuval Yaron; Kathryn Burdon; Ornit Crystal-Shalit; Dvora Kidron; Mira Malcov; Ron Tepper
Journal:  Prenat Diagn       Date:  2007-07       Impact factor: 3.050

8.  Refinement of the X-linked cataract locus (CXN) and gene analysis for CXN and Nance-Horan syndrome (NHS).

Authors:  Simon Brooks; Neil Ebenezer; Subathra Poopalasundaram; Eamonn Maher; Peter Francis; Anthony Moore; Alison Hardcastle
Journal:  Ophthalmic Genet       Date:  2004-06       Impact factor: 1.803

9.  Identification of the gene for Nance-Horan syndrome (NHS).

Authors:  S P Brooks; N D Ebenezer; S Poopalasundaram; O J Lehmann; A T Moore; A J Hardcastle
Journal:  J Med Genet       Date:  2004-10       Impact factor: 6.318

10.  Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes.

Authors:  Annick Toutain; Benoît Dessay; Nathalie Ronce; Maria-Immacolata Ferrante; Julie Tranchemontagne; Ruth Newbury-Ecob; Carina Wallgren-Pettersson; John Burn; Josseline Kaplan; Annick Rossi; Silvia Russo; Ian Walpole; James K Hartsfield; Nina Oyen; Andrea Nemeth; Pierre Bitoun; Dorothy Trump; Claude Moraine; Brunella Franco
Journal:  Eur J Hum Genet       Date:  2002-09       Impact factor: 4.246

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  6 in total

1.  Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing.

Authors:  Nan Hong; Yan-hua Chen; Chen Xie; Bai-sheng Xu; Hui Huang; Xin Li; Yue-qing Yang; Ying-ping Huang; Jian-lian Deng; Ming Qi; Yang-shun Gu
Journal:  J Zhejiang Univ Sci B       Date:  2014-08       Impact factor: 3.066

2.  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 3.  Pediatric cataract: challenges and future directions.

Authors:  Anagha Medsinge; Ken K Nischal
Journal:  Clin Ophthalmol       Date:  2015-01-07

4.  Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing.

Authors:  Alan S Ma; John R Grigg; Gladys Ho; Ivan Prokudin; Elizabeth Farnsworth; Katherine Holman; Anson Cheng; Frank A Billson; Frank Martin; Clare Fraser; David Mowat; James Smith; John Christodoulou; Maree Flaherty; Bruce Bennetts; Robyn V Jamieson
Journal:  Hum Mutat       Date:  2016-01-14       Impact factor: 4.878

5.  A novel small deletion in the NHS gene associated with Nance-Horan syndrome.

Authors:  Huajin Li; Lizhu Yang; Zixi Sun; Zhisheng Yuan; Shijing Wu; Ruifang Sui
Journal:  Sci Rep       Date:  2018-02-05       Impact factor: 4.379

Review 6.  Pediatric cataract.

Authors:  Sudarshan Kumar Khokhar; Ganesh Pillay; Chirakshi Dhull; Esha Agarwal; Manish Mahabir; Pulak Aggarwal
Journal:  Indian J Ophthalmol       Date:  2017-12       Impact factor: 1.848

  6 in total

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