Elsayed Abdelkreem

Elsayed Abdelkreem

Lecturer - Lecturer of Pediatrics

Faculty of medicine

Address: AlShikh-Shibl Village, AlMaragha City, Sohag

Lecturer of Pediatrics at the Faculty of Medicine, Sohag University with a solid medical, research, and teaching experience. Main domains are Pediatric emergencies, critical care, and inherited metabolic diseases. I am interested in developing a career which combines teaching and research, while maintaining my interest in clinical work.

For 5th-year undergraduate medical students: View and download lecture 5 of pediatric emergencies course

2018-11-19 22:40:42

You can view and download LECTURE 4 of pediatric emergencies course entitled "METABOLIC EMERGENCIES & INTOXICATION" by clicking HERE Read more

For 5th-year undergraduate medical students: View and download lecture 4 of pediatric emergencies course

2018-11-13 16:27:06

You can view and download LECTURE 4 of pediatric emergencies course entitled "CARDIOVASCULAR & NEUROLOGICAL EMERGENCIES" by clicking HERE Read more

For 5th-year undergraduate medical students: View and download lecture 3 of pediatric emergencies course

2018-11-12 19:50:05

You can view and download LECTURE 3 of pediatric emergencies course entitled "RESPIRATORY EMERGENCIES" by clicking HERE Read more

For 5th-year undergraduate medical students: View and download lecture 2 of pediatric emergencies course

2018-11-05 16:41:15

You can view and download LECTURE 2 of pediatric emergencies course entitled "PEDIATRIC RESUSCITATION" by clicking HERE Read more

For 5th-year undergraduate medical students: View and download lecture 1 of pediatric emergencies course

2018-10-29 17:51:35

You can view and download LECTURE 1 of pediatric emergencies course entitled "DETECTION OF SERIOUSLY ILL CHILDREN" by clicking here Read more

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Recent advances in understanding beta-ketothiolase (mitochondrial acetoacetyl-CoA thiolase, T2) deficiency

2018-11-08 09:04:28 | Keywords Recent advances, mitochondrial acetoacetyl‑CoA, Beta-ketothiolase deficiency, ACAT1, T2 deficiency,

Beta-ketothiolase (mitochondrial acetoacetyl-CoA thiolase, T2) deficiency (OMIM #203750, *607809) is an inborn error of metabolism that affects isoleucine catabolism and ketone body metabolism. This disorder is clinically characterized by intermittent ketoacidotic crises under ketogenic stresses. In addition to a previous 26-case series, four series of T2-deficient patients were recently reported from different regions. In these series, most T2-deficient patients developed ... Read more

Intronic antisense Alu elements have a negative splicing effect on the inclusion of adjacent downstream exons

2018-08-13 16:33:31 | Keywords Alu elements, Minigene splicing experiment, Splicing factor, Alternative splicing,

Alu elements occupy 10% of the human genome. However, although they contribute to genomic and transcriptomic diversity, their function is still not fully understood. We hypothesized that intronic Alu elements may contribute to alternative splicing. We therefore examined their effect on splicing using minigene constructs including exon 9-exon 11 inclusive of ACAT1 with truncated introns 9 and 10. These constructs ... Read more

Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis

2018-09-16 13:34:47 | Keywords Ketoacidosis, SCOT deficiency, OXCT1, Heterozygous carriers,

Succinyl-CoA:3-oxoacid CoA transferase (SCOT, gene symbol _OXCT1_) deficiency is an autosomal recessive disorder in ketone body utilization that results in severe recurrent ketoacidotic episodes in infancy, including neonatal periods. More than 30 patients with this disorder have been reported and to our knowledge, their heterozygous parents and siblings have had no apparent ketoacidotic episodes. Over 5 years (2008–2012), we investigated ... Read more

Characterization and outcome of 41 patients with beta-ketothiolase deficiency: 10 years' experience of a medical center in northern Vietnam

2018-09-16 13:45:48 | Keywords ACAT1, patient outcome, founder effect, metabolic encephalopathy, T2 deficiency, Ketoacidosis,

Beta-ketothiolase (T2) deficiency is an inherited disease of isoleucine and ketone body metabolism caused by mutations in the _ACAT1_ gene. Between 2005 and 2016, a total of 41 patients with T2 deficiency were identified at a medical center in northern Vietnam, with an estimated incidence of one in 190,000 newborns. Most patients manifested ketoacidotic episodes of varying severity between 6 ... Read more

Two Libyan siblings with beta-ketothiolase deficiency: A case report and review of literature

2018-09-16 13:55:43 | Keywords Mutation, Ketone bodies, Transient expression analysis, ACAT1, metabolic encephalopathy, T2 deficiency,

Beta-ketothiolase (mitochondrial acetoacetyl-CoA thiolase, T2) deficiency is an autosomal recessive disorder characterized by impaired metabolism of ketones and isoleucine. In this study, we report on the first two siblings with T2 deficiency from Libya. Both siblings presented with ketoacidosis, but the severity and outcomes were quite distinctive. T2 deficiency in patient 1, the younger sister, manifested as recurrent severe episodes ... Read more

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Formative assessment

2018-09-29 16:07:13 | Cardiac Examination

Q1- WHICH OF THE FOLLOWING GIVES A MID DIASTOLIC MURMUR? A- Mitral stenosis B- Aortic stenosis C- Ventricular septal defect D- Aortic regurgitation Q2- A MURMUR THAT IS HEARD ALL OVER THE PRECORDIUM, BUT WITHOUT A THRILL WOULD FALL INTO WHICH GRADE? A- Grade III B- Grade II C- Grade IV D- Grade I Q3- VENTRICULAR SEPTAL DEFECTS TYPICALLY PRESENT ... Read more

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Contact me

AddressAlShikh-Shibl Village, AlMaragha City, Sohag
Phone934610421
Emaild.elsayedmohammed@med.sohag.edu.eg

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