According to one definition “intention or gross negligence leading to fabrication of the scientific message or a false credit or emphasis given to scientist’’ is known as forgery or misconduct in science.
Received: December 31, 2018
Accepted: January 28, 2019
doi.org/10.21089/njhs.41.0001
Abstract: WHO proclaims polio a social and community health crisis. Global Polio Eradication Initiative (GPEI) was resolved to make world polio-free and had contributed significantly to eradicate polio from 1000 cases per day in 1988 to 8 per year in 2017.
Received: September 17, 2018
Accepted: January 23, 2019
doi.org/10.21089/njhs.41.0003
Abstract: Background: Hepatitis B and C infections are endemic in Pakistan. The general population has poor knowledge about the HBV vaccine’s availability and the modes of transmission for HBV/HCV.
Received: July 23, 2018
Revised: November 20, 2018
Accepted: November 23, 2018
Abstract: Aims and Objectives: To analyze the data regarding etiological and predisposing factors in pediatric burns and make conclusion for prevention of pediatric burns.
Received: September 19, 2018
Revised: October 31, 2018
Accepted: November 01, 2018
doi.org/10.21089/njhs.41.0014
Qurat-ul-Ain Khan
Abstract: Introduction: The aim of this study was to see the incidence of bedsores in our hospital and determine relating factors.
Received: October 1, 2018
Revised: November 07, 2018
Accepted: November 07, 2018
doi.org/10.21089/njhs.41.0017
Abstract: Introduction: Thalassemia is a common inherited hemoglobinopathy in Pakistan. Despite various preventive measures taken, each year around 5000 new cases are diagnosed. The problem occurs due to undiagnosed beta Thalassemia carriers
Received: September 24, 2018
Revised: October 30, 2018
Accepted: November 01, 2018
doi.org/10.21089/njhs.41.0021
Abstract: Fanconi anemia(FA) is the most common inherited bone marrow failure disorder characterized by cytopenias, somatic defects and increased propensity to develop malignancies.
Received: October 03, 2018
Revised: November 26, 2018
Accepted: November 28, 2018
doi.org/10.21089/njhs.41.0025
CHILD Syndrome
Sejal Neel, Neel Kanth, Raveet Kumar
Abstract: CHILD syndrome is a rare X-linked genetic disorder caused by mutation of NSDHL (NADPH steroid dehydrogenase-like protein) at Xq28 gene. The mutation causes the defective synthesis of cholesterol, which is an important constituent of viscera, hormones etc.
Received: October 1, 2018
Revised: October 24, 2018
Accepted: October 30, 2018
doi.org/10.21089/njhs.41.0031
How We Managed Primary Immunodeficiency Disorders in Pakistan – A Case Based Study
Asifa Noor, Mehjabeen Imam, Tasneem Farzana, Saqib Ansari, Uzma Zaidi, Saima Munzir and Tahir Sultan Shamsi
Introduction: This article emphasizes on the importance of time frame for diagnosis and management of immunodeficiency syndromes and also highlights the diagnostic dilemma that most often such cases are misdiagnosed or undiagnosed which contributes to significant morbidity and mortality
Received: October 03, 2018
Revised: November 15, 2018
Accepted: November 23, 2018
doi.org/10.21089/njhs.41.0034
De Novo Deletion 17p (del17p) in an Adult T-Cell Prolymphocytic Leukemia as a Rare Presentation
Zara-tul-Ain Bashir, Saima Siddiqui, Jawwad Hassan, Tahir Sultan Shamsi
Abstract: T-Cell Prolymphocytic leukemia is a rare and an agressive lymphoproliferative disease which is unresponsive to conventional chemotherapy. We present a case of 72 years old female hospitalized in July 2018 in National Institute of Blood diseases and…
Received: September 3, 2018
Revised: November 20, 2018
Accepted: November 23, 2018
doi.org/10.21089/njhs.41.0042
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