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1-butanol and Congenital Hypothyroidism

1-butanol has been researched along with Congenital Hypothyroidism in 1 studies

1-Butanol: A four carbon linear hydrocarbon that has a hydroxy group at position 1.
butan-1-ol : A primary alcohol that is butane in which a hydrogen of one of the methyl groups is substituted by a hydroxy group. It it produced in small amounts in humans by the gut microbes.

Congenital Hypothyroidism: A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
CHAVARRIA, C1
MUNOS-FERREIRA, G1
GUEVARA, G1
RUPP, JJ1
PASCHKIS, KE1

Other Studies

1 other study available for 1-butanol and Congenital Hypothyroidism

ArticleYear
Butanol-insoluble iodinated compound in the plasma of a goitrous cretin.
    The Journal of clinical endocrinology and metabolism, 1960, Volume: 20

    Topics: 1-Butanol; Butanols; Congenital Hypothyroidism; Goiter; Humans; Iodine; Syndrome

1960