Page last updated: 2024-10-16

adenine and Congenital Hypothyroidism

adenine has been researched along with Congenital Hypothyroidism in 2 studies

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 Excerpts

ExcerptRelevanceReference
"Isolated TSH deficiency is a rare cause of congenital hypothyroidism."1.32Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect. ( Aumann, U; Borck, G; Koch, G; Korsch, E; Martiné, U; Onenli-Mungan, N; Ozer, G; Pfäffle, R; Pohlenz, J; Refetoff, S; Scherberg, NH; Topaloglu, AK; Wildhardt, G; Yuksel, B, 2004)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Borck, G1
Topaloglu, AK1
Korsch, E1
Martiné, U1
Wildhardt, G1
Onenli-Mungan, N1
Yuksel, B1
Aumann, U1
Koch, G1
Ozer, G1
Pfäffle, R1
Scherberg, NH1
Refetoff, S1
Pohlenz, J1
Michelangeli, VP1
Poon, CW1
Arnus, EE1
Frauman, AG1
Connelly, J1
Colman, PG1

Other Studies

2 other studies available for adenine and Congenital Hypothyroidism

ArticleYear
Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect.
    The Journal of clinical endocrinology and metabolism, 2004, Volume: 89, Issue:8

    Topics: Adenine; Child; Child, Preschool; Congenital Hypothyroidism; Female; Founder Effect; Guanine; Haplot

2004
Measurement of TSH receptor blocking immunoglobulins using 3H-adenine incorporation into FRTL-5 and JPO9 cells: use in a child with neonatal hypothyroidism.
    Clinical endocrinology, 1995, Volume: 42, Issue:1

    Topics: Adenine; Antibodies; Binding, Competitive; Biological Assay; Cell Line; Congenital Hypothyroidism; F

1995