نتایج جستجو برای: permanent congenital hypothyroidism

تعداد نتایج: 191616  

2016
Cengiz Kara Figen Günindi Gülay Can Yılmaz Murat Aydın

OBJECTIVE Prevalence of congenital hypothyroidism (CH) in Turkey at birth was reported to be as high as 1:650 in 2008-2010. Incidence rates of permanent and transient CH separately are unknown due to lack of follow-up data. We aimed to evaluate the impact of transient hypothyroidism on increasing incidence of CH and to determine the natural course and the clinical, biochemical, and imaging char...

Journal: :Archives of Disease in Childhood 1978

Journal: :Archives of Disease in Childhood 1986

Journal: :International Journal of Pediatric Endocrinology 2015

Journal: :Archives of Disease in Childhood 1972

Journal: :European journal of endocrinology 2005
Emanuela Medda Antonella Olivieri Maria Antonietta Stazi Michele E Grandolfo Cristina Fazzini Mariangiola Baserga Massimo Burroni Emanuele Cacciari Francesca Calaciura Alessandra Cassio Luca Chiovato Pietro Costa Daniela Leonardi Maria Martucci Lidia Moschini Severo Pagliardini Giuseppe Parlato Alberto Pignero Aldo Pinchera Danielle Sala Lidia Sava Vera Stoppioni Francesco Tancredi Fabiola Valentini Riccardo Vigneri Mariella Sorcini

OBJECTIVE To identify risk factors for permanent and transient congenital hypothyroidism (CH). DESIGN A population-based case-control study was carried out by using the network created in Italy for the National Register of Infants with CH. METHODS Four controls were enrolled for each new CH infant; 173 cases and 690 controls were enrolled in 4 years. In order to distinguish among risk facto...

Journal: :Archives of disease in childhood 1986
J P Chanoine P Bourdoux F Delange

Seven of the 34 infants identified through the Welsh Hypothyroid Screening Programme have additional congenital abnormalities. Two infants have a previously undescribed syndrome, two have chromosomal abnormalities, two have congenital heart disease, and one has a myelomeningocoele. Congenital hypothyroidism often seems to be associated with other congenital abnormalities.

Journal: :European Journal of Pediatrics 2021

Abstract Neonatal screening for congenital primary hypothyroidism (CH) may not distinguish between transient (TCH) and permanent dysfunction (PCH), causing potential overtreatment concerns in affected families. To specify the indication interruption of therapy, we analysed German registry “HypoDok” infants with CH, which oversees 1625 patients from 49 participating centres Germany Austria 1997 ...

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