Zobrazeno 1 - 10
of 94
pro vyhledávání: '"congenital hypothyroidism (CH)"'
Publikováno v:
Journal of Pediatrics Review, Vol 12, Iss 2, Pp 125-142 (2024)
Background: Congenital hypothyroidism (CH) is one of the most prevalent endocrine disorders in children. According to the literature, there is a high prevalence of other anomalies and syndromes in infants diagnosed with CH. Objectives: This study fin
Externí odkaz:
https://doaj.org/article/87fc33ea1c3e4d8a8f49887657ab5563
Autor:
Laura Català, Judit Casas, Sean Yeh, Maria Josa-Eritja, Mireia Tirado-Capistros, Elisenda Moliner, Gemma Carreras
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Congenital hypothyroidism (CH) is the most common cause of endocrinopathy in the newborn Its incidence lies between 1 in 3,000 and 1 in 2,000, However, congenital goiter is a rare form of presentation. Hypothyroidism secondary to autoimmune etiology
Externí odkaz:
https://doaj.org/article/6d6f0e81beb54de7b5c66a6048305a4d
Autor:
Zohar Steinberg Ben-Zeev, Marina Peniakov, Clari Felszer, Scott A Weiner, Avishay Lahad, Shlomo Almashanu, Yardena Tenenbaum Rakover
Publikováno v:
European Thyroid Journal, Vol 11, Iss 4, Pp 1-8 (2023)
Introduction: Maternal thyroid disease is considered as a risk factor for abnormal thyroid function at birth, as well as for long-term morbidity in offspring. The potential harmful effects on the neonate had led to the clinical practice of thyroid fu
Externí odkaz:
https://doaj.org/article/933fe0d4b4f7402b8e7ff92a2b7eea44
Publikováno v:
Endocrines, Vol 3, Iss 1, Pp 107-114 (2022)
Two endocrine disorders, congenital hypothyroidism (CH) and congenital adrenal hyperplasia (CAH), when untreated, can have devastating, irreversible and fatal outcomes. Permanent cognitive impairment, growth failure and dysmorphic appearance are seen
Externí odkaz:
https://doaj.org/article/70f940d215314b6cb9f540d0e0a90c0a
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundsAs a crucial enzyme in thyroid hormone synthesis, the genetic defective thyroid peroxidase (TPO) was one of the main genetic factors leading to congenital hypothyroidism (CH).MethodsMutations in the TPO gene were screened and identified in
Externí odkaz:
https://doaj.org/article/6bb5cc46c5d54ce0a0701e99808b470e
Akademický článek
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Akademický článek
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Autor:
Ralph Fingerhut
Publikováno v:
International Journal of Neonatal Screening, Vol 7, Iss 3, p 51 (2021)
Newborn screening (NBS) for congenital hypothyroidism (CH) started in the 1970s, with the introduction of radioimmuno assays (RIA) for the measurement of thyroxine (T4), and thyroid stimulating hormone (TSH). With the development of sensitive enzyme
Externí odkaz:
https://doaj.org/article/8bd5c1e14ded4c50b374d309b19e7798
Publikováno v:
International Journal of Molecular Sciences
Volume 24
Issue 3
Pages: 2817
Volume 24
Issue 3
Pages: 2817
Newborn screening (NBS) for congenital hypothyroidism (CH) was introduced in Switzerland in 1977, which allowed for the preclinical, biochemical diagnosis. The aim of this study was to evaluate the prevalence of transient CH (tCH) in the canton of Zu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67638ae14008fe6f890b5c133d8c3bea
https://doi.org/10.5167/uzh-231237
https://doi.org/10.5167/uzh-231237
Publikováno v:
International Journal of Neonatal Screening, Vol 6, Iss 1, p 17 (2020)
The purpose of this study was to define reference intervals for total thyroxine (tT4) in dried blood samples (DBSs) obtained for newborn screening. The aim of our study was to assess the possible benefit of measuring tT4 concentrations directly in DB
Externí odkaz:
https://doaj.org/article/c107f92e269c48e0987d86a24fc1b133