International Journal of Pediatrics

Wiedemann-Steiner Syndrome with a 2-Year Follow-Up

Mohamad Hosein Mohamadi; Moein Mobini; Saba Vakili; Rahim Vakili

Volume 10, Issue 10 , October 2022, , Pages 16908-16913

https://doi.org/10.22038/ijp.2022.59825.4654

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

Tyrosinemia Type III: A Case Report with a Seven Years Follow-up

Saba Vakili; Mohammadreza Emami; Moein Mobini; Rahim Vakili

Volume 9, Issue 6 , June 2021, , Pages 13853-13857

https://doi.org/10.22038/ijp.2021.56791.4451

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

Moein Mobini; reza Jafarzadeh Esfehani; Saba Vakili; Ahmadreza Zarifian; Rahim Vakili

Volume 9, Issue 5 , May 2021, , Pages 13503-13513

https://doi.org/10.22038/ijp.2021.56094.4411

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

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Author = Saba Vakili

Wiedemann-Steiner Syndrome with a 2-Year Follow-Up

Abstract

Tyrosinemia Type III: A Case Report with a Seven Years Follow-up

Abstract

Thyroid Disorders in Pediatric Patients with Turner Syndrome; A 16 Years' Experience

Abstract