Genotype-phenotype correlations of dyshormonogenetic goiter in children and adolescents from South India
Background: Dyshormonogenetic goiter is one of the most common causes of hypothyroidism in children and adolescents in iodine nonendemic areas. The exact genotype-phenotypic correlations (GPCs) and risk categorization of hypothyroid phenotypes of dyshormonogenetic mutations are largely speculative....
Main Authors: | Bangaraiah Gari Ramesh, Panchangam Ramakanth Bhargav, Bangaraiah Gari Rajesh, Nangedda Vimala Devi, Rajagopalan Vijayaraghavan, Bhongir Aparna Varma |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2016-01-01
|
Series: | Indian Journal of Endocrinology and Metabolism |
Subjects: | |
Online Access: | http://www.ijem.in/article.asp?issn=2230-8210;year=2016;volume=20;issue=6;spage=816;epage=824;aulast=Ramesh |
Similar Items
-
Dyshormonongenetic goiter: A rare and important entity
by: Yasmin Altaf Momin, et al.
Published: (2020-01-01) -
Persistent goiter with congenital hypothyroidism due to mutation in gene
by: So Yoon Jung, et al.
Published: (2020-03-01) -
Neonatal Dyshormonogenetic Goiter with Hypothyroidism Associated with Novel Mutations in Thyroglobulin and SLC26A4 Gene
by: Valeria Calcaterra, et al.
Published: (2021-05-01) -
Dyshormonogenetic goiter and associated non-thyroidal anomalies
by: Khalid J Farooqui, et al.
Published: (2012-01-01) -
The G395R mutation of the sodium/iodide symporter (NIS) gene in patients with dyshormonogenetic congenital hypothyroidism
by: Neda Mostofizade, et al.
Published: (2013-01-01)