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)
Author = Rahim Vakili
Number of Articles: 19
Wiedemann-Steiner Syndrome with a 2-Year Follow-Up
Volume 10, Issue 10 , October 2022, , Pages 16908-16913
Abstract
Wiedemann-Steiner syndrome (WDSTS) is an exceptionally rare genetic syndrome characterized by postnatal growth retardation, facial dysmorphism, hairy elbow, and short stature. It is ... Read More
A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report
Volume 10, Issue 9 , September 2022, , Pages 16729-16737
Abstract
Background: Short stature is estimated to account for half of the new visits to pediatric endocrine practices. Therefore, evaluating its underlying causes seems essential in order to ... Read More
Prevalence of Testicular Adrenal Rest Tumor and Factors Associated with its Development in 6 Months to 18 Years-old Patients with Congenital Adrenal Hyperplasia
Volume 9, Issue 12 , December 2021, , Pages 15022-15028
Abstract
Background: Congenital adrenal hyperplasia (CAH) is a potentially life-threatening form of primary adrenal insufficiency characterized by cortisol, aldosterone, and epinephrine deficiencies, ... Read More
Tyrosinemia Type III: A Case Report with a Seven Years Follow-up
Volume 9, Issue 6 , June 2021, , Pages 13853-13857
Abstract
Hereditary tyrosinemia type III (OMIM 276710) is a rare inborn error of tyrosine metabolism caused by the deficiency of 4-hydroxyphenylpyruvate dioxygenase (HPD). This ... Read More
Thyroid Disorders in Pediatric Patients with Turner Syndrome; A 16 Years' Experience
Volume 9, Issue 5 , May 2021, , Pages 13503-13513
Abstract
Background Turner syndrome patients are more likely to develop autoimmune diseases in contrast to the general population. Many research have had controversial results suggest a possible ... Read More
The Relation between Karyotype Findings and Gonadotropin Levels in Pediatric Turner’s syndrome Patients
Volume 9, Issue 2 , February 2021, , Pages 13005-13011
Abstract
Background Abnormal pubertal development and fertility are among the frequent complications in Turner’s syndrome. Although elevated level of gonadotropins in Turner’s syndrome ... Read More
Gyrate Atrophy of the Choroid and Retina: A Case Report
Volume 7, Issue 9 , September 2019, , Pages 10119-10123
Abstract
Introduction Gyrate atrophy of the choroid and retina is a metabolic disorder, which is inherited in an autosomal recessive pattern. Although gyrate atrophy is rare, it is concerning ... Read More
Mccune-Albright Syndrome: A Case Report Associated with Pamidronate Therapy and Literature Review
Volume 7, Issue 5 , May 2019, , Pages 9453-9459
Abstract
McCune-Albright Syndrome (MAS) is a rare sporadic disease characterized by bone fibrous dysplasia, Café au lait spots and a variable association of hyperfunction endocrine ... Read More
Papillary Carcinoma Thyroid in a Nine-year-old Child: A Case Report
Volume 6, Issue 8 , August 2018, , Pages 8015-8019
Abstract
Thyroid enlargement and nodules are very rare in children, but when they occur, the chance of malignancy among these nodules is very high. Thyroid carcinoma ... Read More
4-Hydroxybutyric Aciduria as a Rare Presentation of Global Developmental Delay in Children: Case Report of Two Different Patients
Volume 6, Issue 7 , July 2018, , Pages 7861-7865
Abstract
Succinic semialdehyde dehydrogenase (SSADH) deficiency or 4-Hydroxybutyric Aciduria is an autosomal recessive inherited disorder of amma-aminobutyric acid (GABA) degradation. It ... Read More
Lingual Thyroid: A Case Report and Literature Review
Volume 5, Issue 11 , November 2017, , Pages 6049-6055
Abstract
Thyroid ectopia is a dysgenesis of thyroid gland and Lingual position represents the most frequent ectopic location accounting up to 90% of ectopic cases. Hypothyroidism is commonly ... Read More
Black Urine
Volume 4, Issue 6 , June 2016, , Pages 1857-1858
Abstract
A 2-year-old boy was born at term of healthy, non-consanguineous Iranian parents. His mother attended in the clinic with the history of sometimes discoloration of diapers after passing ... Read More
Immunization Coverage in WHO Regions: A Review Article
Volume 3, Issue 2.1 , March 2015, , Pages 111-118
Abstract
In 1974, the World Health Organization (WHO) established the Expanded Program on Immunization (EPI) to ensure that all children have access to routinely recommended ... Read More
McCune-Albright Syndrome: A Case Report and Literature Review
Volume 2, Issue 2.2 , April 2014, , Pages 153-156
Abstract
McCune-Albright syndrome (MAS) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. The disorder is more common in females and is characterized by a triad ... Read More
Maternal Knowledge and Attitude toward Exclusive Breast Milk Feeding (BMF) in the First 6 Months of Infant Life in Mashhad
Volume 2, Issue 1 , January 2014, , Pages 63-69
Abstract
Introduction: Breast milk is a complete food for growing children until 6 months of age, and mothers, as the most important child health care, play a decisive role in their growth. ... Read More
Congenital Rickets: Report of Four Cases
Volume 2, Issue 1 , January 2014, , Pages 101-105
Abstract
Introduction: Vitamin D deficiency and rickets continue to be health problems in developing countries and most of the infants with congenital rickets may present with hypocalcemic seizure. ... Read More
Assessment the Relationship Between Parents' Literacy Level with Children Growth in Mashhad: An Analytic Descriptive Study
Volume 1, Issue 2 , December 2013, , Pages 39-43
Abstract
Introduction: Present children are the investments of community in the future. Preparing children health which leads to the stability of community health, provided to accurate implementation ... Read More
Precocious Puberty: An Unusual Presentation of Hypothyroidism
Volume 1, Issue 2 , December 2013, , Pages 51-54
Abstract
Hypothyroidism is usually associated with delayed pubertal development but in rare occasions precocious puberty may ensue which is seen in cases of prolonged and untreated hypothyroidism. ... Read More
Iron and Multivitamin Supplements in Children and its Association with Growth rate
Volume 1, Issue 1 , August 2013, , Pages 13-17