Perfluoroalkyl substances in serum from South Korean infants with congenital hypothyroidism and healthy infants – Its relationship with thyroid hormones

2016 ◽  
Vol 147 ◽  
pp. 399-404 ◽  
Author(s):  
Da-Hye Kim ◽  
Un-Jung Kim ◽  
Hee-Young Kim ◽  
Sung-Deuk Choi ◽  
Jeong-Eun Oh
Author(s):  
Blanca Sarzo ◽  
Virginia Ballesteros ◽  
Carmen Iñiguez ◽  
Cyntia B. Manzano-Salgado ◽  
Maribel Casas ◽  
...  

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Lin Yang ◽  
Jingguang Li ◽  
Jianqiang Lai ◽  
Hemi Luan ◽  
Zongwei Cai ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Caio Leônidas Oliveira Andrade ◽  
Crésio de Aragão Dantas Alves ◽  
Helton Estrela Ramos

Congenital hypothyroidism (CH) is an endocrine disease commonly found in newborns and is related to the absence or reduction of thyroid hormones (THs), which are essential for development since intrauterine life. Children with CH can develop hearing problems as THs are crucial for the auditory pathway’s development and maturation. Sensory deprivations, especially in hearing disorders at early ages of development, can impair language skills, literacy, and behavioral, cognitive, social, and psychosocial development. In this review we describe clinical and molecular aspects linking CH and hearing loss.


2021 ◽  
Vol 12 ◽  
Author(s):  
Maria C. Opazo ◽  
Juan Carlos Rivera ◽  
Pablo A. Gonzalez ◽  
Susan M. Bueno ◽  
Alexis M. Kalergis ◽  
...  

Fetus and infants require appropriate thyroid hormone levels and iodine during pregnancy and lactation. Nature endorses the mother to supply thyroid hormones to the fetus and iodine to the lactating infant. Genetic variations on thyroid proteins that cause dyshormonogenic congenital hypothyroidism could in pregnant and breastfeeding women impair the delivery of thyroid hormones and iodine to the offspring. The review discusses maternal genetic variations in thyroid proteins that, in the context of pregnancy and/or breastfeeding, could trigger thyroid hormone deficiency or iodide transport defect that will affect the proper development of the offspring.


2018 ◽  
Vol 06 (01) ◽  
pp. e7-e10
Author(s):  
Feride Mehmetoğlu

AbstractRectal atresia is a rare anorectal malformation, and its association with other anomalies is even more rare. This study presents a unique case of co-twin in which the surviving newborn male underwent surgery due to rectal atresia. Newborn screening tests identified congenital hypothyroidism. The surgical treatment consisted of three stages and thyroid hormones were replaced.


2015 ◽  
Vol 77 ◽  
pp. 63-69 ◽  
Author(s):  
Vivian Berg ◽  
Therese Haugdahl Nøst ◽  
Solrunn Hansen ◽  
Astrid Elverland ◽  
Anna-Sofía Veyhe ◽  
...  

2017 ◽  
Vol 222 ◽  
pp. 543-548 ◽  
Author(s):  
Meng-Shan Tsai ◽  
Ching-Chun Lin ◽  
Mei-Huei Chen ◽  
Wu-Shiun Hsieh ◽  
Pau-Chung Chen

2017 ◽  
Vol 220 (4) ◽  
pp. 679-685 ◽  
Author(s):  
Srishti Shrestha ◽  
Michael S. Bloom ◽  
Recai Yucel ◽  
Richard F. Seegal ◽  
Robert Rej ◽  
...  

2018 ◽  
Vol 166 ◽  
pp. 537-543 ◽  
Author(s):  
Samuel C. Byrne ◽  
Pamela Miller ◽  
Samarys Seguinot-Medina ◽  
Vi Waghiyi ◽  
C. Loren Buck ◽  
...  

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