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.
Excerpt | Relevance | Reference |
---|---|---|
"Isolated TSH deficiency is a rare cause of congenital hypothyroidism." | 1.32 | Four 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) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Borck, G | 1 |
Topaloglu, AK | 1 |
Korsch, E | 1 |
Martiné, U | 1 |
Wildhardt, G | 1 |
Onenli-Mungan, N | 1 |
Yuksel, B | 1 |
Aumann, U | 1 |
Koch, G | 1 |
Ozer, G | 1 |
Pfäffle, R | 1 |
Scherberg, NH | 1 |
Refetoff, S | 1 |
Pohlenz, J | 1 |
Michelangeli, VP | 1 |
Poon, CW | 1 |
Arnus, EE | 1 |
Frauman, AG | 1 |
Connelly, J | 1 |
Colman, PG | 1 |
2 other studies available for adenine and Congenital Hypothyroidism
Article | Year |
---|---|
Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect.
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.
Topics: Adenine; Antibodies; Binding, Competitive; Biological Assay; Cell Line; Congenital Hypothyroidism; F | 1995 |