Cargando…

Bilateral combined anterior and posterior lenticonus in Alport’s Syndrome

Alport’s syndrome is an inherited disease characterized by hearing loss, progressive renal failure and ocular abnormalities like anterior lenticonus, corneal opacities, cataract, fleck retinopathies, and temporal retinal thinning. To have anterior and posterior lenticonus in the same eye in this syn...

Descripción completa

Detalles Bibliográficos
Autores principales: Tiwari, Uma Sharan, Aishwarya, Ankita, Kujur, Rashmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Romanian Society of Ophthalmology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256072/
https://www.ncbi.nlm.nih.gov/pubmed/30505993
_version_ 1783374073427918848
author Tiwari, Uma Sharan
Aishwarya, Ankita
Kujur, Rashmi
author_facet Tiwari, Uma Sharan
Aishwarya, Ankita
Kujur, Rashmi
author_sort Tiwari, Uma Sharan
collection PubMed
description Alport’s syndrome is an inherited disease characterized by hearing loss, progressive renal failure and ocular abnormalities like anterior lenticonus, corneal opacities, cataract, fleck retinopathies, and temporal retinal thinning. To have anterior and posterior lenticonus in the same eye in this syndrome is a rare finding and only a few such reports are available. Hereby, we report a case of a 22-year-old male with bilateral combined anterior and posterior lenticonus with sensorineural deafness and nephritis leading to the diagnosis of Alport’s syndrome.
format Online
Article
Text
id pubmed-6256072
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Romanian Society of Ophthalmology
record_format MEDLINE/PubMed
spelling pubmed-62560722018-11-30 Bilateral combined anterior and posterior lenticonus in Alport’s Syndrome Tiwari, Uma Sharan Aishwarya, Ankita Kujur, Rashmi Rom J Ophthalmol Case Reports Alport’s syndrome is an inherited disease characterized by hearing loss, progressive renal failure and ocular abnormalities like anterior lenticonus, corneal opacities, cataract, fleck retinopathies, and temporal retinal thinning. To have anterior and posterior lenticonus in the same eye in this syndrome is a rare finding and only a few such reports are available. Hereby, we report a case of a 22-year-old male with bilateral combined anterior and posterior lenticonus with sensorineural deafness and nephritis leading to the diagnosis of Alport’s syndrome. Romanian Society of Ophthalmology 2018 /pmc/articles/PMC6256072/ /pubmed/30505993 Text en ©Romanian Society of Ophthalmology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Tiwari, Uma Sharan
Aishwarya, Ankita
Kujur, Rashmi
Bilateral combined anterior and posterior lenticonus in Alport’s Syndrome
title Bilateral combined anterior and posterior lenticonus in Alport’s Syndrome
title_full Bilateral combined anterior and posterior lenticonus in Alport’s Syndrome
title_fullStr Bilateral combined anterior and posterior lenticonus in Alport’s Syndrome
title_full_unstemmed Bilateral combined anterior and posterior lenticonus in Alport’s Syndrome
title_short Bilateral combined anterior and posterior lenticonus in Alport’s Syndrome
title_sort bilateral combined anterior and posterior lenticonus in alport’s syndrome
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256072/
https://www.ncbi.nlm.nih.gov/pubmed/30505993
work_keys_str_mv AT tiwariumasharan bilateralcombinedanteriorandposteriorlenticonusinalportssyndrome
AT aishwaryaankita bilateralcombinedanteriorandposteriorlenticonusinalportssyndrome
AT kujurrashmi bilateralcombinedanteriorandposteriorlenticonusinalportssyndrome