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Clinical Relevance of Molecular Diagnosis in Patients with Congenital Hypothyroidism
(OMICS International, 2017-05)
Congenital hypothyroidism, defined as the functional deficiency of thyroid hormones present at birth, occurs in approximately 1: 2,000 to 4,000 newborns. Thyroid hormones play an essential role in the maturation of the ...
Importance of molecular genetic analysis in the diagnosis and classification of congenital hypothyroidism
(Springer, 2014-03)
Congenital hypothyroidism (CH) is the most frequent endocrine disease in infants, with the prevalence ratio in the range of 1:2,000–1:4,000 newborns.
Incidencia de Hipotiroidismo Congénito en 14 Regiones Sanitarias del Paraguay
(Sociedad Paraguaya de Pediatría, 2009)
Phenylketonuria, congenital hypothyroidism and haemoglobinopathies: public health issues for a Brazilian newborn screening programFenilcetonúria, hipotireoidismo congênito e hemoglobinopatias: questões de saúde pública para um programa de triagem neonatal brasileiro
(Escola Nacional de Saúde Pública Sérgio Arouca, 2018)
Congenital hypothyroidism: A diagnosis not to forget
(2012)
Summary: Congenital hypothyroidism (CH) is the most common cause of preventable mental retardation. Since 1994, Chile has a national plan for mass screening all newborns to diagnose the disease. Currently, the CH incidence ...