Literature DB >> 19590516

Variable expressivity of ocular associations of foveal hypoplasia in a family.

A Vincent1, V Kemmanu, R Shetty, V Anandula, B Madhavarao, B Shetty.   

Abstract

PURPOSE: To show the variable expressivity of ocular associations of foveal hypoplasia in three affected members of a family.
METHODS: Three symptomatic members of a family underwent a detailed ophthalmic evaluation including best-corrected distance and near-vision measurement, colour vision assessment, fundus evaluation and fluorescein angiography, horizontal corneal diameter measurement, total axial length measurement, and full-field electroretinogram. Optical coherence tomography was performed in two of the three cases. Pedigree charting was also carried out.
RESULTS: Foveal hypoplasia was shown in all three cases. Pedigree charting showed an autosomal recessive (AR) inheritance pattern of foveal hypoplasia in our series. Microphthalmos and chorioretinal coloboma were found to be variably associated with foveal hypoplasia in this series.
CONCLUSIONS: This interesting case series shows that variable expressivity could be found in AR inheritance patterns of foveal hypoplasia.

Entities:  

Mesh:

Year:  2009        PMID: 19590516     DOI: 10.1038/eye.2009.180

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


  8 in total

1.  Isolated foveal hypoplasia without nystagmus.

Authors:  Audrey Giocanti-Aurégan; Matthew T Witmer; Nathan M Radcliffe; Donald J D'Amico
Journal:  Int Ophthalmol       Date:  2014-01-19       Impact factor: 2.031

2.  Color Vision in Aniridia.

Authors:  Hilde R Pedersen; Lene A Hagen; Erlend C S Landsend; Stuart J Gilson; Øygunn A Utheim; Tor P Utheim; Maureen Neitz; Rigmor C Baraas
Journal:  Invest Ophthalmol Vis Sci       Date:  2018-04-01       Impact factor: 4.799

3.  Posterior Microphthalmia, Peripheral Pigmentary Retinal Changes, Yellow Lesions, and Cleft Lip: A Case Report and Literature Review.

Authors:  Nasser G Alsaedi; Khalid Alrubaie
Journal:  Case Rep Ophthalmol Med       Date:  2019-05-19

4.  The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences.

Authors:  Charlotte C Kruijt; Libe Gradstein; Arthur A Bergen; Ralph J Florijn; Benoit Arveiler; Eulalie Lasseaux; Xavier Zanlonghi; Laura Bagdonaite-Bejarano; Anne B Fulton; Claudia Yahalom; Anat Blumenfeld; Yonatan Perez; Ohad S Birk; Gerard C de Wit; Nicoline E Schalij-Delfos; Maria M van Genderen
Journal:  Invest Ophthalmol Vis Sci       Date:  2022-01-03       Impact factor: 4.799

Review 5.  Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism.

Authors:  James A Poulter; Musallam Al-Araimi; Ivan Conte; Maria M van Genderen; Eamonn Sheridan; Ian M Carr; David A Parry; Mike Shires; Sabrina Carrella; John Bradbury; Kamron Khan; Phillis Lakeman; Panagiotis I Sergouniotis; Andrew R Webster; Anthony T Moore; Bishwanath Pal; Moin D Mohamed; Anandula Venkataramana; Vedam Ramprasad; Rohit Shetty; Murugan Saktivel; Govindasamy Kumaramanickavel; Alex Tan; David A Mackey; Alex W Hewitt; Sandro Banfi; Manir Ali; Chris F Inglehearn; Carmel Toomes
Journal:  Am J Hum Genet       Date:  2013-11-27       Impact factor: 11.025

6.  Isolated foveal hypoplasia: tomographic, angiographic and autofluorescence patterns.

Authors:  Agata Mota; Sofia Fonseca; Angela Carneiro; Augusto Magalhães; Elisete Brandão; Fernando Falcão-Reis
Journal:  Case Rep Ophthalmol Med       Date:  2012-07-31

7.  Absent Foveal Pit, Also Known as Fovea Plana, in a Child without Associated Ocular or Systemic Findings.

Authors:  Laura Hernandez-Moreno; Natacha Moreno Perdomo; Tomas S Aleman; Karthikeyan Baskaran; Antonio Filipe Macedo
Journal:  Case Rep Ophthalmol Med       Date:  2018-07-26

8.  Variable clinical profile of foveal hypoplasia in albinism.

Authors:  Kshitiz Kumar; Subhendu K Boral; Deepak Agarwal; Angshuman Goswami; Tushar K Sinha; Debashish Bhattacharya
Journal:  Indian J Ophthalmol       Date:  2020-04       Impact factor: 1.848

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.