thyroxine has been researched along with De Lange Syndrome in 1 studies
Thyroxine: The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (MONOIODOTYROSINE) and the coupling of iodotyrosines (DIIODOTYROSINE) in the THYROGLOBULIN. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form TRIIODOTHYRONINE which exerts a broad spectrum of stimulatory effects on cell metabolism.
thyroxine : An iodothyronine compound having iodo substituents at the 3-, 3'-, 5- and 5'-positions.
De Lange Syndrome: A syndrome characterized by growth retardation, severe MENTAL RETARDATION, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth, depressed nasal bridge, bushy eyebrows meeting at the midline, hirsutism, and malformations of the hands. The condition may occur sporadically or be associated with an autosomal dominant pattern of inheritance or duplication of the long arm of chromosome 3. (Menkes, Textbook of Child Neurology, 5th ed, p231)
| Excerpt | Relevance | Reference |
|---|---|---|
| "We detected thyroid agenesis which has been never reported in CdLs patients." | 1.46 | Cornelia de lange syndrome with thyroid agenesis of an indonesian patient. ( Fauziah, PN; Hajjah, R; Laksono, B; Maskoen, AM; Nataprawira, HM; Suciati, LP; Zada, A, 2017) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Maskoen, AM | 1 |
| Laksono, B | 1 |
| Hajjah, R | 1 |
| Zada, A | 1 |
| Suciati, LP | 1 |
| Fauziah, PN | 1 |
| Nataprawira, HM | 1 |
1 other study available for thyroxine and De Lange Syndrome
| Article | Year |
|---|---|
Cornelia de lange syndrome with thyroid agenesis of an indonesian patient.
Topics: Cell Cycle Proteins; Congenital Hypothyroidism; De Lange Syndrome; Female; Gene Expression; Humans; | 2017 |