Volume 12 (2024)
Volume 11 (2023)
Volume 10 (2022)
Volume 9 (2021)
Volume 8 (2020)
Volume 7 (2019)
Volume 6 (2018)
Volume 5 (2017)
Volume 4 (2016)
Volume 3 (2015)
Volume 2 (2014)
Volume 1 (2013)
Periorbital Ecthyma Gangrenosum Due to Pseudomonas Aeruginosa Septicemia in an Infant with Sepsis: A Case Report
Periorbital Ecthyma Gangrenosum Due to Pseudomonas Aeruginosa Septicemia in an Infant with Sepsis: A Case Report

Mohammad Etezad Razavi; Seyed Hossein Ghavami Shahri; Farid Shekarchian; Hamid Reza Heidarzadeh; Sepide Hajmohammadi

Volume 10, Issue 7 , July 2022, , Pages 16428-16433

https://doi.org/10.22038/ijp.2022.64385.4887

Abstract
  Purpose: This article aimed to report an infant case of congenital neutropenia (CN) with periorbital ecthyma gangrenosum (EG) due to pseudomonas aeruginosa septicemia.Case report: A ...  Read More
Hemi-Central Retinal Vein Occlusion in a Premature Infant: A Case Report
Hemi-Central Retinal Vein Occlusion in a Premature Infant: A Case Report

Mohammad Reza Ansari Astaneh; Mehrdad Motamed Shariati; Seyed Hossein Ghavami Shahri; Shahin Jahani Maleki; Hamid Reza Heidarzadeh

Volume 10, Issue 6 , June 2022, , Pages 16252-16255

https://doi.org/10.22038/ijp.2022.62301.4768

Abstract
  Background: This study reports the case of an infant patient with organized vitreous hemorrhage (VH) due to hemi-central retinal vein occlusion (Hemi-CRVO) secondary to thrombocytosis.Case ...  Read More
A Case Report of Glucose-Galactose Malabsorption in Iranian Child
A Case Report of Glucose-Galactose Malabsorption in Iranian Child

Pantea Tajik; Amir Hossein Goudarzian; Zeinab Pourzahabi

Volume 7, Issue 5 , May 2019, , Pages 9399-9403

https://doi.org/10.22038/ijp.2019.35793.3124

Abstract
  Introduction Glucose-Galactose Malabsorption (GGM) is an autosomal recessive and rare disorder of intestinal transport of glucose and sodium-glucose cotransporter type (SGLT1). Case ...  Read More
A Case Report of Schimke Immuno-Osseous Dysplasia: A Rare Autosomal Recessive Disorder
A Case Report of Schimke Immuno-Osseous Dysplasia: A Rare Autosomal Recessive Disorder

Banafsheh Arad; Zahra Pirzadeh

Volume 6, Issue 2 , February 2018, , Pages 7151-7155

https://doi.org/10.22038/ijp.2017.26522.2282

Abstract
        Schimke immune-osseous dysplasia (SIOD) is a rare autosomal recessive disorder presented with specific facial features, skeletal dysplasia, steroid resistance ...  Read More
A Carcinoid Tumor of the Appendix in a Child: A Case Report
A Carcinoid Tumor of the Appendix in a Child: A Case Report

Laleh Vahedi Larijani; Seyed Abdollah Mousavi; Somayyeh Sheidaie

Volume 6, Issue 1 , January 2018, , Pages 6891-6895

https://doi.org/10.22038/ijp.2017.27646.2389

Abstract
  The appendix is one of the most common sites for carcinoid tumors. Most carcinoids are found in appendices removed incidentally at laparotomy for conditions unrelated to acute appendicitis. ...  Read More
Fetus in Fetus in the Sacral Sac: Report of Surgical Management Case
Fetus in Fetus in the Sacral Sac: Report of Surgical Management Case

Halim Berdi Taneh; Maryam Chehrehgosha; Ghorban Mohammad Kochaki; Soheila Kalantari; Seyyed Nima Naleini

Volume 6, Issue 1 , January 2018, , Pages 6963-6969

https://doi.org/10.22038/ijp.2017.25826.2201

Abstract
  Background: Fetus-In-Fetu (FIF) is a rare congenital malformation, which consists of a fetus mixed with a distinct tissue that is from the other fetus of twin. FIF is defined as a mass ...  Read More
Ecballium Elaterium Poisoning in Pediatric Emergency Service: A Case Report
Ecballium Elaterium Poisoning in Pediatric Emergency Service: A Case Report

Sinem Sarı Gökay; Özlem Tolu Kendir; Hayri Levent Yılmaz

Volume 6, Issue 1 , January 2018, , Pages 6977-6980

https://doi.org/10.22038/ijp.2017.26634.2292

Abstract
  BackgroundEcballium elaterium is the only species belonging to the genus Ecballium of Cucurbitaceae family. It is native to the Mediterranean region. Despite its side effects, E. elaterium ...  Read More
A Case of Pulmonary Foreign Body Reviewed as Mass
A Case of Pulmonary Foreign Body Reviewed as Mass

Seyed Javad Sayedi; Reza Shojaeian; Maliheh Bani Hassan; Ali Khakshour

Volume 4, Issue 8 , August 2016, , Pages 2281-2286

https://doi.org/10.22038/ijp.2016.7326

Abstract
  Foreign Body Aspiration (FBA) is a common and sometimes life-threatening problem in children and in higher age groups. FBA highest incidence rate is during the second year in children ...  Read More
Report of Four Children with Gaucher Disease and Review of Literature
Report of Four Children with Gaucher Disease and Review of Literature

Wajiha Maan; Manoochehr Karjoo; Mirza Beg

Volume 4, Issue 8 , August 2016, , Pages 2287-2293

https://doi.org/10.22038/ijp.2016.7307

Abstract
  Gaucher Disease (GD) is the most common type of Lysosomal Storage Disorder and it is divided into three distinct subtypes. The authors here report four different cases of Gaucher Disease, ...  Read More
Idiopathic Stevens-Johnson Syndrome in a Child: a Case Report
Idiopathic Stevens-Johnson Syndrome in a Child: a Case Report

Amir Hossein Goudarzian; Mahya Ghahramanlou; Sina Ehsani; Ali Abbaskhanian; Afshin Shourofi

Volume 4, Issue 7 , July 2016, , Pages 2113-2117

https://doi.org/10.22038/ijp.2016.7035

Abstract
  Background Stevens-Johnson syndrome (SJS) is one of potentially fatal disorders that often occur after taking certain types of medication. There are reports of this disease after some ...  Read More
Living with Colicky Infant and New Modalities: a Case Report
Living with Colicky Infant and New Modalities: a Case Report

Ali Reza Mansourzadeh; Soheil Najafi Mehri

Volume 4, Issue 7 , July 2016, , Pages 2241-2246

https://doi.org/10.22038/ijp.2016.7152

Abstract
  Parents who have a baby with infantile colic experienced a different thought and emotions such as hopelessness, fatigue and impasses. In this study, our living experience as a professional ...  Read More
Immunoproliferative Small Intestine Disease (IPSID): A Case Report
Immunoproliferative Small Intestine Disease (IPSID): A Case Report

Farid Imanzadeh; Aliakbar Sayarri; Pantea Tajik

Volume 3, Issue 2.1 , March 2015, , Pages 89-92

https://doi.org/10.22038/ijp.2015.4056

Abstract
  Immunoproliferative small intestinal disease (IPSID) is the syndrome associated with Mediterranean lymphoma (a rare form of non-Hodgkin’s lymphoma). Many of the patients diagnosed ...  Read More