Literature DB >> 15002027

Ophthalmic features of Turner's syndrome.

A K O Denniston1, L Butler.   

Abstract

Turner's syndrome is one of the most common of all chromosomal abnormalities and is associated with significant ophthalmic morbidity. Turner's 1938 account included two patients with strabismus, and hitherto the condition has generated more interest among orthoptists than ophthalmologists. This systematic review of the literature seeks to redress the balance. Based on the pooled data of 274 patients with Turner's syndrome, it is the most complete evaluation so far of the prevalence and severity of ophthalmic problems in this population. This includes both a systematic review of the ophthalmic literature (via Medline) and the much larger body of work available in the orthoptic literature. Finally, we consider recent progress that enables the ophthalmologist to progress from the simple recognition of a phenotype to the correlation of genotypic variations with embryogenesis and consequent features of that phenotype.

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Mesh:

Year:  2004        PMID: 15002027     DOI: 10.1038/sj.eye.6701323

Source DB:  PubMed          Journal:  Eye (Lond)        ISSN: 0950-222X            Impact factor:   3.775


  7 in total

1.  [Analysis of an ophthalmic pathology cohort of human fetal eyes with regard to interesting findings].

Authors:  M C Herwig; A M Müller; F G Holz; K U Loeffler
Journal:  Ophthalmologe       Date:  2010-11       Impact factor: 1.059

2.  Detection of a congenital cystic eyeball by prenatal ultrasound in a newborn with Turner's syndrome.

Authors:  Marsha C Kavanagh; Diamond Tam; Jennifer J Diehn; Anthony Agadzi; Edward L Howes; Douglas R Fredrick
Journal:  Br J Ophthalmol       Date:  2007-04       Impact factor: 4.638

3.  Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol).

Authors:  Elodie Fiot; Bertille Alauze; Bruno Donadille; Dinane Samara-Boustani; Muriel Houang; Gianpaolo De Filippo; Anne Bachelot; Clemence Delcour; Constance Beyler; Emilie Bois; Emmanuelle Bourrat; Emmanuel Bui Quoc; Nathalie Bourcigaux; Catherine Chaussain; Ariel Cohen; Martine Cohen-Solal; Sabrina Da Costa; Claire Dossier; Stephane Ederhy; Monique Elmaleh; Laurence Iserin; Hélène Lengliné; Armelle Poujol-Robert; Dominique Roulot; Jerome Viala; Frederique Albarel; Elise Bismuth; Valérie Bernard; Claire Bouvattier; Aude Brac; Patricia Bretones; Nathalie Chabbert-Buffet; Philippe Chanson; Regis Coutant; Marguerite de Warren; Béatrice Demaret; Lise Duranteau; Florence Eustache; Lydie Gautheret; Georges Gelwane; Claire Gourbesville; Mickaël Grynberg; Karinne Gueniche; Carina Jorgensen; Veronique Kerlan; Charlotte Lebrun; Christine Lefevre; Françoise Lorenzini; Sylvie Manouvrier; Catherine Pienkowski; Rachel Reynaud; Yves Reznik; Jean-Pierre Siffroi; Anne-Claude Tabet; Maithé Tauber; Vanessa Vautier; Igor Tauveron; Sebastien Wambre; Delphine Zenaty; Irène Netchine; Michel Polak; Philippe Touraine; Jean-Claude Carel; Sophie Christin-Maitre; Juliane Léger
Journal:  Orphanet J Rare Dis       Date:  2022-07-12       Impact factor: 4.303

4.  Turner syndrome and associated problems in Turkish children: a multicenter study.

Authors:  Ediz Yeşilkaya; Abdullah Bereket; Feyza Darendeliler; Firdevs Baş; Şükran Poyrazoğlu; Banu Küçükemre Aydın; Şükran Darcan; Bumin Dündar; Muammer Büyükinan; Cengiz Kara; Erkan Sarı; Erdal Adal; Ayşehan Akıncı; Mehmet Emre Atabek; Fatma Demirel; Nurullah Çelik; Behzat Özkan; Bayram Özhan; Zerrin Orbak; Betül Ersoy; Murat Doğan; Ali Ataş; Serap Turan; Damla Gökşen; Ömer Tarım; Bilgin Yüksel; Oya Ercan; Şükrü Hatun; Enver Şimşek; Ayşenur Ökten; Ayhan Abacı; Hakan Döneray; Mehmet Nuri Özbek; Mehmet Keskin; Hasan Önal; Nesibe Akyürek; Kezban Bulan; Derya Tepe; Hamdi Cihan Emeksiz; Korcan Demir; Deniz Kızılay; Ali Kemal Topaloğlu; Erdal Eren; Samim Özen; Saygın Abalı; Leyla Akın; Beray Selver Eklioğlu; Sultan Kaba; Ahmet Anık; Serpil Baş; Tolga Ünüvar; Halil Sağlam; Semih Bolu; Tolga Özgen; Durmuş Doğan; Esra Deniz Çakır; Yaşar Şen; Nesibe Andıran; Filiz Çizmecioğlu; Olcay Evliyaoğlu; Gülay Karagüzel; Özgür Pirgon; Gönül Çatlı; Hatice Dilek Can; Fatih Gürbüz; Çiğdem Binay; Veysel Nijat Baş; Kürşat Fidancı; Adem Polat; Davut Gül; Cengizhan Açıkel; Hüseyin Demirbilek; Peyami Cinaz; Carolyn Bondy
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-03

5.  A Rare Case of Unilateral Morning Glory Disc Anomaly in a Patient with Turner Syndrome: Report and Review of Posterior Segment Associations.

Authors:  Dev R Sahni; Michael Wallace; Mansi Kanhere; Hind Al Saif; Natario Couser
Journal:  Case Rep Ophthalmol Med       Date:  2018-06-28

6.  Nationwide Study of Turner Syndrome in Ukrainian Children: Prevalence, Genetic Variants and Phenotypic Features

Authors:  Nataliya Zelinska; Iryna Shevchenko; Evgenia Globa
Journal:  J Clin Res Pediatr Endocrinol       Date:  2018-02-28

7.  Homozygous mutation in ABCA4 associated with cone rod dystrophy in a patient with Turner syndrome.

Authors:  Yousra Falfoul; Imen Habibi; Ahmed Turki; Achraf Ben Yakhlef; Khaled El Matri; Ahmed Chebil; Nibrass Chaker; Daniel Schorderet; Leila El Matri
Journal:  Tunis Med       Date:  2021-02
  7 in total

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