Results 1 to 10 of about 29,638 (237)

Congenital hypothyroidism in pediatric practice

open access: yesМедицинский совет, 2016
We present observation of two patients with congenital hypothyroidism. Importance of neonatal screening for congenital hypothyroidism is demonstrated.The main principles of diagnostics, therapy and dispensary supervision, role of pediatricians in ...
A. V. Vitebskaya, T. V. Igamberdieva
doaj   +3 more sources

Information Registry System on Congenital Hypothyroidism: A Systematic Review

open access: yesJournal of Pediatrics Review, 2021
Background: Congenital hypothyroidism is the most common congenital disorder of the endocrine system, leading to preventable mental retardation. Objectives: We aimed to evaluate the current status of congenital hypothyroidism information registry ...
Morteza Ghasempour   +4 more
doaj   +1 more source

A 7-year study on the prevalence of congenital hypothyroidism in northern Iran

open access: yesElectronic Physician, 2018
Background: Congenital hypothyroidism (CH) is one of the most common congenital endocrine disorders. The present study determined the prevalence and demographic characteristics of congenital hypothyroidism in the north of Iran. Objective: To determine
Zahra Beheshti   +4 more
doaj   +1 more source

SCREENING FOR CONGENITAL HYPOTHYROIDISM [PDF]

open access: yesPediatric Research, 1975
The early diagnosis of congenital hypothyroidism relies essentially on the biological evidence of the defect. Preliirinary data of a systematic screening of neonates are presented. The values of serum thyroxine (T4) and TSH were determined in the cord blood of 271 infants.
Winkler, M.   +2 more
openaire   +2 more sources

The Importance of Examining Congenital Hypothyroidism in Connection with Congenital Heart Disease: Letter to Editor [PDF]

open access: yesIranian Journal of Neonatology, 2019
Dear Editor-in-Chief: I read and enjoyed your stylish article, "Frequency of Congenital Cardiac Malformations in Neonates with Congenital Hypothyroidism", in relation to heart disease with hypothyroidism.
Forod Salehi   +2 more
doaj   +1 more source

An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism, 2020
Alport syndrome (AS) is a rare genetic disorder that causes progressive nephritis and is more common among males. Studies have reported an association between thyroid antibodies and hypothyroidism in patients with AS, but the relevance of this ...
Su-Jeong Lee   +4 more
doaj   +1 more source

Characteristics of thyroid nodules in infant with congenital hypothyroidism [PDF]

open access: yesKorean Journal of Pediatrics, 2014
PurposeThis study aimed to assess the characteristics of thyroid nodules among infants diagnosed with congenital hypothyroidism.MethodsA retrospective study of 660 infants (374 males, 286 females) diagnosed with congenital hypothyroidism was carried out ...
Seo Young Youn   +3 more
doaj   +1 more source

Untreated Congenital Hypothyroidism Mimicking Hirschsprung Disease: A Puzzling Case in a One-Year-Old Child

open access: yesCase Reports in Pediatrics, 2018
Congenital hypothyroidism is a clinical emergency due to its potential risk of mental retardation. Constipation might be present in hypothyroid children. However, Hirschsprung disease is rarely associated with congenital hypothyroidism. Herein, a case of
Soraia Tahan   +6 more
doaj   +1 more source

Statistical data analysis of the risk factors of Neonatal Congenital Hypothyroidism in Khuzestan Province, Iran

open access: yesData in Brief, 2018
This article contains data on the effective factors on congenital hypothyroidism (CH) that was learned from a case-control study designed in Khuzestan province in Iran. The data set of this article provides information on newborn descriptive features and
Yousef Alimohamadi   +2 more
doaj   +1 more source

Genetics of congenital hypothyroidism [PDF]

open access: yesJournal of Medical Genetics, 2005
Congenital hypothyroidism is the most common neonatal metabolic disorder and results in severe neurodevelopmental impairment and infertility if untreated. Congenital hypothyroidism is usually sporadic but up to 2% of thyroid dysgenesis is familial, and congenital hypothyroidism caused by organification defects is often recessively inherited.
S M, Park, V K K, Chatterjee
openaire   +2 more sources

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