Literature DB >> 35450195

Association of type II Waardenburg syndrome with hypermetropic amblyopia.

Shee Wen Chua1,2, Safinaz Mohd Khialdin1, Mushawiahti Mustapha1, Norshamsiah Md Din1, Meng Hsien Yong1.   

Abstract

Entities:  

Year:  2022        PMID： 35450195      PMCID： PMC8995733          DOI： 10.18240/ijo.2022.04.26

Source DB:  PubMed          Journal:  Int J Ophthalmol        ISSN： 2222-3959            Impact factor:   1.779


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  9 in total

Review 1.  Waardenburg syndrome.

Authors:  A P Read; V E Newton
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

2.  Anisometropic amblyopia in a case of type 2 Waardenburg syndrome.

Authors:  Ali Akal; Tugba Göncü; Nurefsan Boyaci; Ömer Faruk Yılmaz
Journal:  BMJ Case Rep       Date:  2013-12-18

3.  Heterogeneity in Waardenburg's syndrome. Report of a family with ocular albinism.

Authors:  L A Bard
Journal:  Arch Ophthalmol       Date:  1978-07

Review 4.  Clinical findings in Japanese patients with Waardenburg syndrome type 2.

Authors:  Naonori Ohno; Motohiro Kiyosawa; Hiroshi Mori; Wei Fang Wang; Hiroshi Takase; Manabu Mochizuki
Journal:  Jpn J Ophthalmol       Date:  2003 Jan-Feb       Impact factor: 2.447

5.  Ophthalmological screening of a paediatric cochlear implant population: a retrospective analysis and 12-year follow-up.

Authors:  K Falzon; M Guerin; T Fulcher; L Viani
Journal:  Eye (Lond)       Date:  2009-10-16       Impact factor: 3.775

6.  Tietz/Waardenburg type 2A syndrome associated with posterior microphthalmos in two unrelated patients with novel MITF gene mutations.

Authors:  Vianney Cortés-González; Juan Carlos Zenteno; Martín Guzmán-Sánchez; Verónica Giordano-Herrera; Dalia Guadarrama-Vallejo; Narlly Ruíz-Quintero; Cristina Villanueva-Mendoza
Journal:  Am J Med Genet A       Date:  2016-09-08       Impact factor: 2.802

7.  Waardenburg Syndrome: A Case Study of Two Patients.

Authors:  Karan Sharma; Archana Arora
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2015-06-29

8.  New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing.

Authors:  Wu Li; Lingyun Mei; Hongsheng Chen; Xinzhang Cai; Yalan Liu; Meichao Men; Xue Zhong Liu; Denise Yan; Jie Ling; Yong Feng
Journal:  Neural Plast       Date:  2019-02-27       Impact factor: 3.599

9.  Whole genome genotyping mapped regions on chromosome 2 and 18 in a family segregating Waardenburg syndrome type II.

Authors:  Maan Abdullah Albarry; Ahdab Qasem Alreheli; Alia M Albalawi; Sulman Basit
Journal:  Saudi J Ophthalmol       Date:  2019-09-18
  9 in total

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