Publications by authors named "Amr Sharaf"

Article Synopsis
  • The study investigates the presence of candiduria (yeast in urine) in critically ill patients with solid or hematological cancers, analyzing its predictive factors and impact on patient outcomes.
  • The research included 173 patients, finding that 16.8% had candiduria, primarily caused by non-albicans Candida species, with previous antibiotic use and specific medical interventions identified as key risk factors.
  • Candiduria was linked to significantly higher mortality rates in the ICU, indicating that it serves as a marker of increased clinical severity in these patients.
View Article and Find Full Text PDF

Aim Of The Work: To evaluate the incidence and risk factors for development of retinopathy of prematurity (ROP) in the biggest neonatal intensive care unit (NICU) in Itay Elbaroud City, Behera province, Egypt.

Methods: We studied data of 240 newly born infants with gestational age (GA) ≤34 weeks or birth weight (BW) ≤2000 g or infants with unstable course who were admitted to the biggest NICU in Itay Elbaroud City, Behera province, Egypt, 
between October 1, 2018 and October 31, 2020. There is no standard screening system in Egypt.

View Article and Find Full Text PDF

Purpose: To investigate the safety and efficacy of green thermal laser as an adjunctive therapy for the treatment of resistant infectious keratitis (IK) in the Delta region of Egypt.

Methods: A retrospective case series of 150 patients, within a 4 year duration, with resistant IK, who failed to respond to specific medical treatment alone for 7 days, were included. They all received green thermal laser photocoagulation treatment to the cornea as an adjunctive to medical treatment.

View Article and Find Full Text PDF

Oral-facial-digital syndrome type 1 (OMIM #311200) is an X-linked dominant, developmental disorder. Among the 13 described clinical variants of oral-facial-digital syndrome, oral-facial-digital syndrome type 1 is of significance to dermatologists due to presence of congenital milia and hypotrichosis, not described in other variants. Since oral-facial-digital syndrome type 1 is genetically a distinct entity, awareness of these features help to clinically delineate this from other variants.

View Article and Find Full Text PDF