Traumatic hyphaema and sickle cell retinopathy in a patient with sickle cell-haemoglobin E (HbSE) disease

Author:

Ganesh Anuradha,AI-Habsi Nassra S M,AI-Alawi Fatma K A,Mitra Sandip,Eriksson Anders,Venugopalan Poothirikovil

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Reference14 articles.

1. Crouch ER, Williams PB . Trauma: ruptures and bleeding. In: Tasman W, Jaeger EA, editors. Duane's clinical ophthalmology. Philadelphia: JB Lippincott, 1993:1–22.

2. Nasrullah A, Kerr NC . Sickle cell trait as a risk factor for secondary haemorrhage in children with traumatic hyphaema. Am J Ophthalmol 1997;123:783–90.

3. Zimmerman TJ, Kooner KS, Sharir M, Fechtner R . Textbook of ocular pharmacology. Philadelphia: Lippincott-Raven, 1997.

4. Serjeant GR . Sickle cell disease. Oxford: Oxford University Press, 1992.

5. Vishwanathan C, Agarwal MB, Bichille LS, Bhave AB . Double heterozygosity for hemoglobin S and E. Indian Pediatr 1992;29:895–7.

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1. Acute chest syndrome in sickle cell disease/HBE patient, A case report;Clinical Case Reports;2021-08

2. Manifestations of HbSE sickle cell disease: a systematic review;Journal of Translational Medicine;2021-06-16

3. Hemoglobin SE Disease in Hatay, in the Southern Part of Turkey;Thalassemia Reports;2015-02-24

4. First Reported Case of Proliferative Retinopathy in Hemoglobin SE Disease;Case Reports in Ophthalmological Medicine;2014

5. Hemoglobin SE disease—A concise review;American Journal of Hematology;2007-07

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