Results 41 to 50 of about 208,465 (197)
Nature Communications, 2023 The pathogenesis of thyroid dysgenesis (TD) is not well understood. Here, using a combination of single-cell RNA and spatial transcriptome sequencing, we identify a subgroup of NF-κB-activated thyrocytes located at the center of thyroid tissues in ...
Rui-Meng Yang +16 more
doaj +1 more source
An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism [PDF]
Annals 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
Prevalence of thyroid dysgenesis according to sex and laterality.
, 2019 Prevalence of thyroid dysgenesis according to sex and laterality.
Hideki Hattori (7325933) +8 more
core +1 more source
, 2014 Context: Congenital hypothyroidism (CH), the most frequent endocrine congenital disease, can occur either based on a thyroid hormone biosynthesis defect or can predominantly be due to thyroid dysgenesis.
BEREKET, ABDULLAH +2 more
core +2 more sources
Journal of Behçet Uz Children's Hospital, 2022 Objective: In this study, we aimed to determine the frequency and etiology of transient and permanent congenital hypothyroidism (CH), and to investigate the role of laboratory data in predicting permanent and transient hypothyroidism.
Özlem Nalbantoğlu, Behzat Özkan
doaj +1 more source
Resistance to Thyroid Hormone Beta: A Focused Review
Frontiers in Endocrinology, 2021 Resistance to thyroid hormone (RTH) is a clinical syndrome defined by impaired sensitivity to thyroid hormone (TH) and its more common form is caused by mutations in the thyroid hormone receptor beta (THRB) gene, termed RTHβ.
Theodora Pappa, Samuel Refetoff
doaj +1 more source
Diffential diagnostics and genealogical features of congential hypothyroidism in childrens
Клиническая и экспериментальная тиреоидология, 2007 Congenital hypothyroidism (CH) being one of the most frequent thyroid disorder among children is etiologically heterogeneous. In this study various etiological forms of primary CH (ectopic thyroid gland, athyreosis, hypoplasia, dyshormonogenesis) were ...
doaj +1 more source
Andrology, EarlyView.ABSTRACT Background Familial clustering of testicular germ cell tumour (TGCT) is well‐established, whereas the risk of non‐testicular cancer among relatives remains inconsistent across studies. Objective To evaluate the overall and site‐specific cancer risk among first‐degree relatives and grandparents of TGCT patients compared to cancer‐free controls.
Csilla Krausz +13 more
wiley +1 more source
Congenital hypothyroidism after newborn screening program reorganization in the Apulia region
Italian Journal of Pediatrics, 2022 Background Congenital hypothyroidism (CH) is the most frequent congenital endocrine disorder. The purpose of the present study was to evaluate the incidence and etiological classification of CH in Apulia in a three-year period according to the ...
Simonetta Simonetti +9 more
doaj +1 more source
Andrology, EarlyView.ABSTRACT Background Since the 1990s, declining sperm counts and increasing testicular cancer rates have raised worldwide concern about male reproductive health, including in Denmark. This prompted a prospective population‐based study with annual surveillance of semen quality.
Lærke Priskorn +13 more
wiley +1 more source