Protein tyrosine phosphatase non-receptor type 22 C1858T gene polymorphism in children with down syndrome and autoimmune thyroid diseases

Protein tyrosine phosphatase non-receptor type 22 C1858T gene polymorphism in children with down syndrome and autoimmune thyroid diseases

Autoimmune Thyroid Disease (AIT) is a frequent comorbidity in Down Syndrome (DS). Protein Tyrosine Phosphatase Non- Receptor Type 22 C1858T (PTPN-22 C1858T) gene polymorphisms have a role in the progression of AIT. The study on PTPN- 22 C1858T gene polymorphism as the risk factor of AIT in DS child...

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Bibliographic Details
Main Authors: Muhammad Faizi, Nur Rochmah, Soetjipto Soetjipto, Anang Endaryanto, Sukmawati Basuki, Yuni Hisbiyah, Rayi Kurnia Perwitasari
Format: Article
Language:English
Published: PAGEPress Publications 2023-02-01
Series:La Pediatria Medica e Chirurgica
Subjects:
PTPN-22 C1858T polymorphism
hypothyroidism
down syndrome
autoimmunity
Online Access:https://pediatrmedchir.org/pmc/article/view/283

Internet

https://pediatrmedchir.org/pmc/article/view/283

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