Sudanese Journal of Paediatrics 2019, Volume 19, No. 1
Editorial Board
TABLE OF CONTENTS
About the cover
Mustafa Abdalla M. Salih pp1-1
Editorial
The odyssey of diagnosing genetic disorders in evolving health services
Mustafa Abdalla M. Salih, Mohammed Osman Swar pp2-5
Review
Coeliac disease in children: the need to improve awareness in resource-limited settings
Siba Prosad Paul, Lauren Katie Stanton, Helen Louise Adams, Dharamveer Basude pp6-13
Original Articles
Seroprevelence of rubella among children suspected of having measles in Gadarif Hospital, Eastern Sudan
Mohammed Ahmed A. Ahmed, Ahmed Mohamedain, AbdelAziem A. Ali, Ishag Adam pp14-18
Effect of colostrum given within the 12 hours after birth on feeding outcome, morbidity and mortality in very low birth weight infants: a prospective cohort study
Tanveer Bashir, Kallem Venkat Reddy, Sai Kiran, Srinivas Murki, Dattatray Kulkarni, Pawale Dinesh pp19-24
Renal scarring following urinary tract infections in children
Balakrishna Bandari, Seema Pavaman Sindgikar, Soma Santosh Kumar, Mangalpady Shenoy Vijaya, Raghu Shankar pp25-30
Lactulose versus polyethylene glycol for disimpaction therapy in constipated children, a randomized controlled study
Mohammad Salem Shatnawi, Mohammad Mu azi Alrwala, Abdulla Majed Ghanma, Mohammad Lutfi Alquraan, Ehab Nequla Zreiqat, Manar Mohammad Alzoubi pp31-36
Infantile Supratentorial Subdural Empyema Managed By Percutaneous Aspiration: An Outcome Study In A Nigerian City
Okezie Obasi Kanu, Christopher I. Esezobor, Omotayo A. Ojo, Chinyere N. Asoegwu, Chinenye Nnoli, Yusuf D. Dawang, Edamisan Temiye pp37-43
Insight into potassium’s role in childhood mortality due to severe acute malnutrition
Sumia M. S. Alasad, Omaima Abdelmajeed Mohamed Salih, Mahmoud Hassan pp44-51
Short Communication
Importance of pedigree in patients with familial epilepsy and intellectual disability
Huseyin Caksen, Fesih Aktar, Gokcen Yildirim, Serdar Ceylaner pp52-56
Karyotype analysis in children with idiopathic intellectual disability
Huseyin Caksen, Hayrettin Okut, Mevlit Ikbal pp57-59
Case Reports
Coexistence of genetic conditions: Exploring a possible relationship
Bothainah Alaqeel, Amir Babakir, Fuad Al Mutairi, Mohammed Al Dubayee pp60-66
A rare cutaneous manifestation of Kawasaki disease
Abdulmajeed Abdulrahman Alfadhel, Jubran Theeb Alqanatis pp67-70
Image
Type II growing skull fracture in a 12 year old girl
Sunil Malik, Sonal Saran, Tanvi Khanna, Reema Gupta pp71-74
Disclaimer
Editorial Board
TABLE OF CONTENTS
About the cover
Mustafa Abdalla M. Salih pp1-1
Editorial
The odyssey of diagnosing genetic disorders in evolving health services
Mustafa Abdalla M. Salih, Mohammed Osman Swar pp2-5
Review
Coeliac disease in children: the need to improve awareness in resource-limited settings
Siba Prosad Paul, Lauren Katie Stanton, Helen Louise Adams, Dharamveer Basude pp6-13
Original Articles
Seroprevelence of rubella among children suspected of having measles in Gadarif Hospital, Eastern Sudan
Mohammed Ahmed A. Ahmed, Ahmed Mohamedain, AbdelAziem A. Ali, Ishag Adam pp14-18
Effect of colostrum given within the 12 hours after birth on feeding outcome, morbidity and mortality in very low birth weight infants: a prospective cohort study
Tanveer Bashir, Kallem Venkat Reddy, Sai Kiran, Srinivas Murki, Dattatray Kulkarni, Pawale Dinesh pp19-24
Renal scarring following urinary tract infections in children
Balakrishna Bandari, Seema Pavaman Sindgikar, Soma Santosh Kumar, Mangalpady Shenoy Vijaya, Raghu Shankar pp25-30
Lactulose versus polyethylene glycol for disimpaction therapy in constipated children, a randomized controlled study
Mohammad Salem Shatnawi, Mohammad Mu azi Alrwala, Abdulla Majed Ghanma, Mohammad Lutfi Alquraan, Ehab Nequla Zreiqat, Manar Mohammad Alzoubi pp31-36
Infantile Supratentorial Subdural Empyema Managed By Percutaneous Aspiration: An Outcome Study In A Nigerian City
Okezie Obasi Kanu, Christopher I. Esezobor, Omotayo A. Ojo, Chinyere N. Asoegwu, Chinenye Nnoli, Yusuf D. Dawang, Edamisan Temiye pp37-43
Insight into potassium’s role in childhood mortality due to severe acute malnutrition
Sumia M. S. Alasad, Omaima Abdelmajeed Mohamed Salih, Mahmoud Hassan pp44-51
Short Communication
Importance of pedigree in patients with familial epilepsy and intellectual disability
Huseyin Caksen, Fesih Aktar, Gokcen Yildirim, Serdar Ceylaner pp52-56
Karyotype analysis in children with idiopathic intellectual disability
Huseyin Caksen, Hayrettin Okut, Mevlit Ikbal pp57-59
Case Reports
Coexistence of genetic conditions: Exploring a possible relationship
Bothainah Alaqeel, Amir Babakir, Fuad Al Mutairi, Mohammed Al Dubayee pp60-66
A rare cutaneous manifestation of Kawasaki disease
Abdulmajeed Abdulrahman Alfadhel, Jubran Theeb Alqanatis pp67-70
Image
Type II growing skull fracture in a 12 year old girl
Sunil Malik, Sonal Saran, Tanvi Khanna, Reema Gupta pp71-74
Disclaimer