A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report

BACKGROUND: The retinopathy is an uncommon complication in individuals with sickle cell trait except for the cases of sickle cell trait associated with systemic arterial hypertension, diabetes mellitus, syphilis, tuberculosis and sarcoidosis. CASE PRESENTATION: A retinopathy in a 16 year-old child w...

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Autores principales: Ouzzif, Zohra, El Maataoui, Aissam, Traore, Zeinab, Biaz, Asmae, El Machtani, Samira, Dami, Abdellah, Bouhsain, Sanae, Messaoudi, Nezha, Benchrifa, Fatiha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5242008/
https://www.ncbi.nlm.nih.gov/pubmed/28100178
http://dx.doi.org/10.1186/s12886-017-0402-x
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author Ouzzif, Zohra
El Maataoui, Aissam
Traore, Zeinab
Biaz, Asmae
El Machtani, Samira
Dami, Abdellah
Bouhsain, Sanae
Messaoudi, Nezha
Benchrifa, Fatiha
author_facet Ouzzif, Zohra
El Maataoui, Aissam
Traore, Zeinab
Biaz, Asmae
El Machtani, Samira
Dami, Abdellah
Bouhsain, Sanae
Messaoudi, Nezha
Benchrifa, Fatiha
author_sort Ouzzif, Zohra
collection PubMed
description BACKGROUND: The retinopathy is an uncommon complication in individuals with sickle cell trait except for the cases of sickle cell trait associated with systemic arterial hypertension, diabetes mellitus, syphilis, tuberculosis and sarcoidosis. CASE PRESENTATION: A retinopathy in a 16 year-old child with no history of consanguinity in the parents revealed a sickle S trait associated to heterozygous alpha thalassemia. His mother has Sickle cell anaemia (Hb SS) and his father is a carrier of heterozygous alpha-thalassemia status that it was unknown before. CONCLUSION: This case report describes a proliferative retinopathy in a 16 year-old patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait.
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spelling pubmed-52420082017-01-23 A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report Ouzzif, Zohra El Maataoui, Aissam Traore, Zeinab Biaz, Asmae El Machtani, Samira Dami, Abdellah Bouhsain, Sanae Messaoudi, Nezha Benchrifa, Fatiha BMC Ophthalmol Case Report BACKGROUND: The retinopathy is an uncommon complication in individuals with sickle cell trait except for the cases of sickle cell trait associated with systemic arterial hypertension, diabetes mellitus, syphilis, tuberculosis and sarcoidosis. CASE PRESENTATION: A retinopathy in a 16 year-old child with no history of consanguinity in the parents revealed a sickle S trait associated to heterozygous alpha thalassemia. His mother has Sickle cell anaemia (Hb SS) and his father is a carrier of heterozygous alpha-thalassemia status that it was unknown before. CONCLUSION: This case report describes a proliferative retinopathy in a 16 year-old patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait. BioMed Central 2017-01-18 /pmc/articles/PMC5242008/ /pubmed/28100178 http://dx.doi.org/10.1186/s12886-017-0402-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Ouzzif, Zohra
El Maataoui, Aissam
Traore, Zeinab
Biaz, Asmae
El Machtani, Samira
Dami, Abdellah
Bouhsain, Sanae
Messaoudi, Nezha
Benchrifa, Fatiha
A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report
title A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report
title_full A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report
title_fullStr A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report
title_full_unstemmed A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report
title_short A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report
title_sort retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5242008/
https://www.ncbi.nlm.nih.gov/pubmed/28100178
http://dx.doi.org/10.1186/s12886-017-0402-x
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