Results 61 to 70 of about 679,172 (179)
Orphanet Journal of Rare Diseases, 2021 Introduction The clinical complications of congenital hypothyroidism such as brain disorders are very subtle and are not recognizable in infancy period. They are recognizable when it is too late for treatment or prevention.
Javad Nazari +8 more
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, 2022 Hypothyroidism is an endocrine disorder commonly caused by Hashimoto’s disease. Nowadays, autoimmune diseases appear to be on the rise. As such, there is renewed interest in hypothyroidism. This book presents a comprehensive overview of the disorder with
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Congenital central hypothyroidism in a neonate born to thyrotoxic mother
Journal of Integrated Health Sciences, 2016 Maternal thyrotoxicosis is associated with significant risk of low birth weight premature & small for gestational age neonates; as well as intrauterine death.
M N Rasania, P M Modi
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Etiological evaluation of primary congenital hypothyroidism cases
, 2017 Aim: Primary congenital hypothyroidism is frequently seen endocrine disorder and one of the preventable cause of mental retardation. Aim of study was to evaluate the frequency of permanent/transient hypothyrodism, and to detect underlying reason to ...
Nese Torun +7 more
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Etiology of congenital hypothyroidism in Isfahan: Does it different?
Advanced Biomedical Research, 2014 Background: Considering the higher prevalence of congenital hypothyroidism (CH) in Iran and the importance of determination of the etiology of CH for assessing appropriate treatment strategies, understanding the pathogenesis of CH and the implications of
Mahin Hashemipour +9 more
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71 INCIDENCE OF THYROID ANTIBODIES IN NEWBORNS WITH PERMANENT CONGENITAL HYPOTHYROIDISM [PDF]
Pediatric Research, 1985 The influence of maternal autoimmune thyroid disease and placental transfer of antithyroid antibodies has been discussed as one cause of congenital hypothyroidism. In order to evaluate this hypothesis thyroid microsomal antibodies(anti-M), thyroglobulin antibodies (anti-T) and TSH-receptor antibodies(anti-TSH-R) were determined in serum samples of 36 ...
Annette Grüters +6 more
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Permanent congenital hypothyroidism with blood spot thyroid stimulating hormone <10 mU/L
, 2017 Background: The UK recommended lower threshold for neonatal blood spot thyroid stimulating hormone (TSH) screening for congenital hypothyroidism (CHT) is 10.0 mU/L. Some laboratories use lower thresholds.
Mason, Avril +4 more
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Frontiers in EndocrinologyImportanceSubacute thyroiditis (SAT) is a self-limiting and inflammatory thyroid disease. Although SAT usually improves on its own within weeks, it needs treatment when patients have pain, fever, and symptoms of thyrotoxicosis.
Anqi Yuan, Jialu Wu, Hui Huang
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Graves' Disease: Can It Be Cured? [PDF]
Endocrinology and Metabolism, 2019 Whether or not Graves' hyperthyroidism can be really cured, depends on the definition of “cure.” If eradication of thyroid hormone excess suffices for the label “cure,” then all patients can be cured because total thyroidectomy or high doses of 131I will
Wilmar M. Wiersinga
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Screening for congenital hypothyroidism in Maltese newborns using cord blood [PDF]
, 1996 Routine screening for congenital hypothyroidism (CHT) has been introduced because clinical features of CHT may not be evident before the baby is a few weeks old and treatment at this stage may already be too late.
Rizzo, M. +3 more
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