Results 101 to 110 of about 940,867 (195)
Neonatal Screening for Congenital Hypothyroidism in West Black Sea Area in Turkey
The aim of this study was to investigate the incidence of congenital hypothyroidism (CH) in The West Black Sea Area, a mild to moderate iodine deficient area in Turkey.
Enver Şimşek +2 more
doaj +2 more sources
Congenital hypothyroidism: information for parents
"08/22/13.""Congenital hypothyroidism (CH) is a condition that affects infants from birth (congenital) and results from a partial or complete loss of thyroid function (hypothyroidism ...
Kansas Newborn Screening Program
core +1 more source
Efeito do T3 reverso sobre o estresse oxidativo induzido pelo hipotireoidismo congênito em hipocampo de ratos imaturos: envolvimento de mecanismos não genômicos [PDF]
Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Programa de Pós-Graduação em Farmácia, Florianópolis, 2014.Abstract : Congenital hypothyroidism can lead to a variety of neurochemical and morphophysiological ...
Domingues, Juliana Tonietto
core
Background: The prevalence of congenital hypothyroidism (CH) is high in Isfahan (Iran). Considering the high rate of parental consanguinity and the role of dual oxidase 2 (DUOX2) gene in transient and permanent CH due to thyroid dyshormonogenesis, the ...
Omid Khoshnoud +8 more
doaj
An Unusual Presentation of Congenital Hypothyroidism in a Newborn: Transient Pseudo-Obstruction [PDF]
Congenital hypothyroidism is mostly asymptomatic at birth. It is usually detected by targeted neonatal screening for CH that is performed after birth. Nonetheless, there are reports of rare and vague presentations of CH, as protracted icterus, abdominal distension, skin mottling, hypoactivity, poor feeding, muscle hypotonia, huge posterior fontanel ...
openaire +1 more source
High risk of congenital hypothyroidism in multiple pregnancies.
CONTEXT: In Italy, the surveillance of congenital hypothyroidism (CH) is performed by the Italian National Registry of Infants with CH (INRICH). Up to now, about 3600 infants with CH are recorded in the INRICH, and a high number of twins are included ...
Stazi MA +10 more
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Werdnig-Hoffmann disease with congenital hypothyroidism
Congenital hypothyroidism is often associated with other congenital anomalies. In some instances it is difficult to differentiate congenital hypothyroidism from Werdnig-Hoffmann's disease.
Kurtoglu, Selim +4 more
core +1 more source
Key Points Congenital hypothyroidism (CH) is the most common preventable cause of intellectual disability. Prompt diagnosis and recognition are critical to support optimal neurodevelopmental outcomes and overall growth.The newborn ...
Alexa Durante +2 more
core +1 more source
. Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism. The New England journal of medicine, 347(2), 95-102.
Mutations, Congenital
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TRANSIENT FAMILIAL CONGENITAL HYPOTHYROIDISM: ABOUT A SIBLING OF THREE
Introduction:Congenitalhypothyroidismis one of the mostcommonpreventable causes of intellectualdisability. It isclassifiedinto permanent and transient. The transientdisorderrefers to atemporarydeficiency of thyroid hormones at birth but thenrecovering to normal thyroid hormone production.Wewillpresent a case of congenitalhypothyroidism in a sibling of
Dassoufi Rania +3 more
openaire +1 more source

