Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Primary congenital hypothyroidism"'
Autor:
Valeria Calcaterra, Rossella Lamberti, Claudia Viggiano, Sara Gatto, Luigina Spaccini, Gianluca Lista, Gianvincenzo Zuccotti
Publikováno v:
Pediatric Reports, Vol 13, Iss 2, Pp 210-215 (2021)
Congenital goiter is an uncommon cause of neck swelling and it can be associated with hypothyroidism. We discuss a case of primary hypothyroidism with goiter presenting at birth. Ultrasound showed the enlargement of the gland and thyroid function tes
Externí odkaz:
https://doaj.org/article/b03b858bac0d40bdb5ae4967b118142a
Autor:
Buffler, Patricia A., Kelsh, Michael A., Lau, Edmund C., Edinboro, Charlotte H., Barnard, Julie C., Rutherford, George W., Daaboul, Jorge J., Palmer, Lynn, Lorey, Fred W.
Publikováno v:
Environmental Health Perspectives, 2006 May 01. 114(5), 798-804.
Externí odkaz:
https://www.jstor.org/stable/3651057
Autor:
Claudia Viggiano, Gianluca Lista, Valeria Calcaterra, Luigina Spaccini, Rossella Lamberti, Gian Vincenzo Zuccotti, Sara Gatto
Publikováno v:
Pediatric Reports, Vol 13, Iss 29, Pp 210-215 (2021)
Pediatric Reports
Pediatric Reports
Congenital goiter is an uncommon cause of neck swelling and it can be associated with hypothyroidism. We discuss a case of primary hypothyroidism with goiter presenting at birth. Ultrasound showed the enlargement of the gland and thyroid function tes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f833724f105c0dfa36b1817b3dc29c5
https://www.mdpi.com/2036-7503/13/2/29
https://www.mdpi.com/2036-7503/13/2/29
Akademický článek
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Publikováno v:
Клиническая и экспериментальная тиреоидология, Vol 6, Iss 2, Pp 40-45 (2010)
Primary congenital hypothyroidism (CH) is the most common neonatal metabolic disorder and before the introduction of neonatal screening programs it was one of the most frequent causes of mental retardation. CH has the incidence of about 1:3000 newbor
Externí odkaz:
https://doaj.org/article/c5414a6bb9f9419d9ceed0ac4b0f302c
Autor:
Abeer Al-Sofyani, Saud F. Alshaikh, Meshari A. Turjoman, Eman Althobaiti, Anwar Borai, Seham Alameer, Feras Badriq, Mohammed Mujalled
Publikováno v:
Journal of Clinical Laboratory Analysis
Background Cord‐blood and heel‐prick TSH levels are essential in diagnosing and preventing the serious complications of congenital hypothyroidism, which mainly include intellectual disability. The study aimed to compare between cord‐blood and h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa92600d8a717606f545d68e0305b2c9
https://pubmed.ncbi.nlm.nih.gov/34859927
https://pubmed.ncbi.nlm.nih.gov/34859927
Autor:
E. A. Troshina, A. A. Rybakova, S. I. Kutsev, N. М. Platonova, E. A. Panfilova, P. O. Osmanova
Publikováno v:
Arhivʺ Vnutrennej Mediciny, Vol 9, Iss 5, Pp 367-372 (2019)
Background: In the Russian Federation, newborn screening comprises thyroid stimulating hormone determination to exclude primary congenital hypothyroidism. Screening is carried out throughout Russia. Neonatal TSH can be used to assess iodine deficienc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c744a297eb1b0bc560afcc926e52c4d1
https://doi.org/10.20514/2226-6704-2019-9-5-367-372
https://doi.org/10.20514/2226-6704-2019-9-5-367-372
Autor:
Paul B Kaplowitz
Publikováno v:
Pediatric Clinics of North America. 66:343-352
"Thyroid dysfunction that requires prompt diagnosis and treatment often becomes evident in the newborn period because of testing that is done as part of universal newborn screening. Primary congenital hypothyroidism is the most common treatable cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c95495a6203f676418a30baca7be68dc
https://doi.org/10.1016/j.pcl.2018.12.005
https://doi.org/10.1016/j.pcl.2018.12.005
Autor:
Liliana Fernández-Hernández, Carmen Sánchez, Aidy González-Núñez, Ariadna González-del Angel, Miguel Angel Alcántara-Ortigoza, Iraís Sánchez-Verdiguel, Rosario Moreno-Rojas, Víctor Martínez-Cruz
Publikováno v:
Journal of Pediatric Genetics. :041-046
Congenital hypothyroidism (CH), attributable to thyroid dysgenesis (TD), has an unusually high prevalence in Mexican population but the causes are unknown. NKX2-1, as a candidate gene, was subjected to automated Sanger sequencing in 122 unrelated Mex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38e8783910f83488c085fbb203cdabf5
https://doi.org/10.1055/s-0038-1676644
https://doi.org/10.1055/s-0038-1676644
Autor:
Norbert Jorch, Markus Bettendorf, Tilman R Rohrer, Reinhard W. Holl, Nicola Matejek, Holger Haberland, Joachim Wölfle, K. O. Schwab, Eva-Maria Busemann, Sascha R. Tittel
Publikováno v:
European Journal of Pediatrics
Neonatal screening for congenital primary hypothyroidism (CH) may not distinguish between transient (TCH) and permanent dysfunction (PCH), causing potential overtreatment and concerns in affected families. To specify the indication for interruption o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1c5ba1edc441f87e35121ec15790f23
https://doi.org/10.21203/rs.3.rs-219858/v1
https://doi.org/10.21203/rs.3.rs-219858/v1
