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F Betancourt

Publications and source records attributed to F Betancourt.

4 recordsLinked to original sources

Retinopathy in haemoglobin C trait.

Retinopathy associated with sickle-C and sickle cell disease is well described. Sickle trait and haemoglobin C trait are generally considered benign conditions, with infrequent systemic manifestations. Rare cases of retinopathy in sickle trait, in the presence of contributory factors, exist and we recently reported three such patients. The occurrence of retinopathy in haemoglobin C trait is even less well documented. Haemoglobin C does not cause red blood cell sickling but is known to decrease erythrocyte plasticity and increase blood viscosity. We report three cases in which haemoglobin C trait was associated with significant peripheral vascular occlusion and seafan formation (confirmed by fluorescein angiography) similar to that seen in sickle retinopathy. Two patients had coexistent systemic disease (hypertension and diabetes mellitus). Vitreous haemorrhage was the presenting feature in two patients. It is evident that haemoglobin C trait may be associated with sight-threatening complications.

Adult↗

Presumed occlusion of posterior ciliary arteries following central retinal vein decompression surgery.

OBJECTIVE: Sectioning of the posterior scleral ring has been advocated in the treatment of central retinal vein occlusion. We reviewed cases in which this surgery apparently produced sectioning or closure of the short and long posterior ciliary arteries that resulted in a triangular area of choroidal ischemia and permanent chorioretinal lesions. DESIGN: Case series. SETTING: Clinic-based vitreoretinal referral practice. PATIENTS: Four eyes of three patients whose ages ranged from 17 to 53 years underwent sectioning of the posterior scleral rings as treatment for central retinal vein occlusion. MAIN OUTCOME MEASURES: Findings from complete ophthalmologic evaluation. RESULTS: All patients had either an oval or a triangular area of choroidal ischemia nasal to the optic disc and had permanent chorioretinal lesions. CONCLUSIONS: Valid basis for performing this operation requires further investigation.

Adolescent↗

[Wilson's disease].

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Ceruloplasmin↗