Literature DB >> 15557865

[Retinopathy as a sickle-cell trait: myth or reality?].

A Fany1, S Boni, C Adjorlolo, M L Toure Konan, K Gbe, F Coulibaly, R Berete.   

Abstract

INTRODUCTION: The retinopathy of sickle cell diseases is an ischemic retinopathy that occurs frequently in the major forms of HbSS and HbSC sickle cell diseases. The retinopathy of sickle trait HbAS has not been described extensively. PATIENTS AND METHODS: The aim of this study was to describe the retinal characteristics and thus gain better knowledge of sickle trait HbAS retinopathy. Seventy HbAS patients had a complete ocular examination including fluorescein angiography.
RESULTS: Seventy percent of the patients had retinal lesions, with 49.3% non-vasoproliferative lesions, 22.7% prevasoproliferative lesions and 2.7% neovascular lesions. DISCUSSION AND
CONCLUSION: Retinopathy is associated with the HbAS sickle cell trait, but it is less serious than in the major forms of sickle cell syndrome.

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Year:  2004        PMID: 15557865     DOI: 10.1016/s0181-5512(04)96259-6

Source DB:  PubMed          Journal:  J Fr Ophtalmol        ISSN: 0181-5512            Impact factor:   0.818


  1 in total

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

Authors:  Zohra Ouzzif; Aissam El Maataoui; Zeinab Traore; Asmae Biaz; Samira El Machtani; Abdellah Dami; Sanae Bouhsain; Nezha Messaoudi; Fatiha Benchrifa
Journal:  BMC Ophthalmol       Date:  2017-01-18       Impact factor: 2.209

  1 in total

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