Results 111 to 120 of about 940,867 (195)

Rare case of hypothyroidism in a child

Клинический разбор в общей медицине
Hypothyroidism is a decrease or complete loss of thyroid function. In childhood, congenital hypothyroidism is the most common, which can be either permanent or transient.
Tatyana V. Kovalenko, Irina N. Petrova , Liaisan M. Mullakhmetova   +2 more
doaj   +1 more source

Thyroid Gene Mutations in Pregnant and Breastfeeding Women Diagnosed With Transient Congenital Hypothyroidism: Implications for the Offspring's Health. [PDF]

Front Endocrinol (Lausanne), 2021
Opazo MC, Rivera JC, Gonzalez PA, Bueno SM, Kalergis AM, Riedel CA.   +5 more
europepmc   +1 more source

Intelligence quotient in children with congenital hypothyroidism: The effect of diagnostic and treatment variables

Journal of Research in Medical Sciences, 2013
Background: Considering the high prevalence of congenital hypothyroidism (CH) in Isfahan, the intelligence quotient (IQ) of children with CH and the effect of diagnostic and treatment variables on it were investigated during the CH screening program ...
Seyed Badredin Najmi, Mahin Hashemipour, Mohammad Reza Maracy, Silva Hovsepian, Mahmood Ghasemi   +4 more
doaj  

50 YEARS OF NEWBORN SCREENING FOR CONGENITAL HYPOTHYROIDISM: EVOLUTION OF INSIGHTS IN ETIOLOGY, DIAGNOSIS AND MANAGEMENT: Transient or permanent congenital hypothyroidism: from milestones to current and future perspectives

European Thyroid Journal
Primary congenital hypothyroidism (CH) is the most common endocrinopathy of developmental age. In recent years, several studies from different countries have reported a significant increase in CH incidence detected by newborn screening programs ...
Gaia Vincenzi, Ilenia Teresa Petralia, Marco Abbate, Maria Cristina Vigone   +3 more
doaj   +1 more source

Transient congenital hypothyroidism [PDF]

Archives of Disease in Childhood, 1987
openaire   +1 more source

Alphafetoprotein in screening for congenital hypothyroidism

, 2001
171-180This study was conducted on 500 full-term neonates and 25 older patients with congenital hypothyroidism [CH], newly or previously diagnosed. Alphafetoprotein [AFP] was elevated in two neonates.
Abdel Fattah, S., Osman, A., Rafik, M.M., El Din Azzam, M.E., Shawky, R.M.   +4 more
core  

Prevalence of Concurrent Congenital Disabilities in Infants With Congenital Hypothyroidism: A Systematic Review [PDF]

Journal of Pediatrics Review
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.
Mahin Hashemipour, Jila Yousofi, Rojin Chegini, Silva Hovsepian   +3 more
doaj  

Does Congenital Hypothyroidism Have Different Etiologies in Iran? [PDF]

, 2011
Objective: To determine the prevalence of congenital hypothyroidism (CH), permanent and transient CH. Methods: From November 2006 to September 2007, 63031 newborns were screened by measuring serum TSH obtained by heel prick.
Amirhakimi, Gholamhossein, Mohammadi, Hamid, Sanei-far, Heidyeh, Dalili, Setillia, Karamizadeh, Zohre, Karamifard, Hamdollah   +5 more
core  

Cyclic alternating pattern in infants with congenital hypothyroidism

, 2019
Congenital hypothyroidism is defined as thyroid hormone deficiency present at birth which is crucial for brain development. Recently, the cyclic alternating pattern, a rhythm present in electroencephalography recordings in non-Rapid eye movement sleep ...
Poblano, Adrian, Alvarado Ruiz, Gerardo Alberto, Bruni, Oliviero, Rojas-Zamorano, José Ángel, Velazquez-Moctezuma, Javier, Santana-Miranda, Rafael, Dominguez-Salazar, Emilio, Castillo Montoya, Carlos Raúl, Esqueda-León, Enrique, Murata, Chiharu, Rosa, Agostinho   +10 more
core   +1 more source

Clinical and genetic insights into congenital hypothyroidism with gland-in-situ

Trends in Pediatrics
Objective: This study aimed to investigate the genetic etiology of congenital hypothyroidism (CH) with gland-in-situ (GIS) by screening 23 candidate genes using next-generation sequencing (NGS) in a cohort of Turkish patients.
Fatma Dursun, Metin Eser, Murat Hakkı Yarar, Irmak Dicle Sargın, Ayşe Yaşar, Esma Ebru Altun, Fatma Güliz Atmaca, Şerife Ece Ulu, Heves Kırmızıbekmez   +8 more
doaj   +1 more source