This cross-sectional study explored and generated novel and useable estimates of association between variants within genes underlying the transmethylation and trans-sulphuration pathways and inter-individual phenotypic variation in sickle cell anaemia (HbSS).
This study investigated the association of radiological abnormalities and asymptomatic bacteriuria in patients with sickle cell disease. No association was seen and there was no increased risk of symptomatic urinary tract infections in these patients.
ABSTRACT
Objective: The prevalence of asymptomatic bacteriuria (ASB) in sickle cell disease (SCD) in Jamaica is 5.3%. This study sought to determine the association between ASB and anatomical urological abnormalities and symptomatic urinary tract infections (UTIs).
This retrospective case series reports on low rates of fractures in males on androgen deprivation for prostate cancer in Jamaica.
ABSTRACT
Objective: Androgen deprivation therapy (ADT) reduces bone mineral density in men treated for prostate cancer. We sought to determine if there was an ethnic difference in fractures induced by ADT in Jamaican men.
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This report represents a retrospective case series of males with sickle cell disease who have recurrent episodes of ischaemic priapism and were being treated with hydroxyurea for other indications. We evaluated the changes in priapism episodes in these patients.
This paper reports on obstetric outcomes of subjects, diagnosed with subclinical hypothyroidism, who were treated with l-thyroxine, and seeks to determine if these outcomes were equivalent to those of euthyroid subjects.
ABSTRACT
Objective: Restoration of euthyroidism with l-thyroxine reportedly reduces obstetric complications associated with subclinical hypothyroidism (SCH). The objective was to determine if obstetric outcomes of treated subjects were equivalent to euthyroid subjects.
Sickle cell disease still carries a high morbidity and mortality in patients admitted to hospital. Recurrent admissions are a concern, as this impact on patient’s morbidity and quality of life.
ABSTRACT
Objective: To determine the clinical factors associated with the length of hospitalization and mortality in patients with sickle cell disease (SCD).