phenytoin has been researched along with Congenital Hypothyroidism in 3 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Postellon, DC | 1 |
| Sakurada, T | 1 |
| Yamaguchi, T | 1 |
| Yamamoto, M | 1 |
| Tayama, S | 1 |
| Demura, H | 1 |
| Wu, NF | 1 |
| Kushnick, T | 1 |
1 review available for phenytoin and Congenital Hypothyroidism
| Article | Year |
|---|---|
Diagnosis and treatment of congenital hypothyroidism.
Topics: Cholestyramine Resin; Congenital Hypothyroidism; Drug Interactions; Female; Humans; Hypothyroidism; | 1983 |
2 other studies available for phenytoin and Congenital Hypothyroidism
| Article | Year |
|---|---|
[Radioimmunoassay of triiodothyronine].
Topics: Congenital Hypothyroidism; Dinitrophenols; Humans; Hyperthyroidism; Hypothyroidism; Iodine Isotopes; | 1972 |
The Beckwith-Wiedemann syndrome. The exomphalos-macroglossia-gigantism syndrome.
Topics: Abnormalities, Multiple; Blood Glucose; Brain Damage, Chronic; Congenital Hypothyroidism; Diagnosis, | 1974 |