Neonatal screening for congenital hypothyroidism: results and perspectives. Hormone research | Zendy

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Neonatal screening for congenital hypothyroidism: results and perspectives. Hormone research

Author(s) -

F Delange

Publication year - 2000

Publication title -

problems of endocrinology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.124

H-Index - 5

eISSN - 2308-1430

pISSN - 0375-9660

DOI - 10.14341/probl11835

Subject(s) - congenital hypothyroidism , in utero , medicine , hormone , pediatrics , brain development , thyroid , thyroid hormones , mental development , endocrinology , physiology , fetus , pregnancy , psychology , biology , developmental psychology , neuroscience , genetics

Congenital hypothyroidism (HB) is detected in 1 out of 4,000 newborns [1, 2]. G is one of the most common diseases in pediatric endocrinology [3 |, as well as one of the most common cases of reversible brain damage and mental retardation in industrial countries. The delay in mental development in hepatitis A is associated with the fact that thyroid hormones take an active part in the development of the brain | 4], the formation of which occurs in utero and in the early postnatal period until the 2nd or 3rd year of life [5].

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