triiodothyronine has been researched along with Albright Syndrome in 6 studies
Triiodothyronine: A T3 thyroid hormone normally synthesized and secreted by the thyroid gland in much smaller quantities than thyroxine (T4). Most T3 is derived from peripheral monodeiodination of T4 at the 5' position of the outer ring of the iodothyronine nucleus. The hormone finally delivered and used by the tissues is mainly T3.
3,3',5-triiodo-L-thyronine : An iodothyronine compound having iodo substituents at the 3-, 3'- and 5-positions. Although some is produced in the thyroid, most of the 3,3',5-triiodo-L-thyronine in the body is generated by mono-deiodination of L-thyroxine in the peripheral tissues. Its metabolic activity is about 3 to 5 times that of L-thyroxine. The sodium salt is used in the treatment of hypothyroidism.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Thyroid crisis is even rare in patients with MAS, and we report the clinical outcomes of the first case of a MAS patient with atypical triiodothyronine (T3) hyperthyroidism who developed thyroid crisis after orthopedic surgery." | 8.12 | Postoperative thyroid crisis in an 11-year old male with McCune-Albright syndrome and atypical triiodothyronine hyperthyroidism: A case report. ( Hu, C; Hu, J, 2022) |
| "A 17-year-old girl with McCune-Albright syndrome (MAS) was suspected of having central hypothyroidism based on an inappropriately normal thyroid-stimulating hormone (TSH) and low free thyroxine (fT4)." | 7.81 | Low serum free thyroxine level in a girl with McCune-Albright syndrome. ( Pajuväli, A; Peet, A; Roosimaa, M; Tillmann, V, 2015) |
| "McCune-Albright syndrome (MAS) is caused by mutations in GNAS (most often R201C or R201H) leading to constitutive cAMP signaling and multiple endocrine dysfunctions, including morphological and functional thyroid involvement." | 5.35 | The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3,5,3'-triiodothyronine toxicosis of McCune-Albright syndrome. ( Brillante, BA; Celi, FS; Cherman, N; Chidakel, A; Collins, MT; Coppotelli, G; Feuillan, PP; Kelly, M; Shawker, T, 2008) |
| " Thyroid crisis is even rare in patients with MAS, and we report the clinical outcomes of the first case of a MAS patient with atypical triiodothyronine (T3) hyperthyroidism who developed thyroid crisis after orthopedic surgery." | 4.12 | Postoperative thyroid crisis in an 11-year old male with McCune-Albright syndrome and atypical triiodothyronine hyperthyroidism: A case report. ( Hu, C; Hu, J, 2022) |
| "A 17-year-old girl with McCune-Albright syndrome (MAS) was suspected of having central hypothyroidism based on an inappropriately normal thyroid-stimulating hormone (TSH) and low free thyroxine (fT4)." | 3.81 | Low serum free thyroxine level in a girl with McCune-Albright syndrome. ( Pajuväli, A; Peet, A; Roosimaa, M; Tillmann, V, 2015) |
| "To identify the molecular defect by which psychomotor retardation is caused in two brothers with congenital hypothyroidism who received adequate treatment with l-thyroxine." | 3.72 | A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy. ( Ahrens, W; Hiort, O; Pohlenz, J, 2003) |
| "McCune-Albright syndrome (MAS) is caused by mutations in GNAS (most often R201C or R201H) leading to constitutive cAMP signaling and multiple endocrine dysfunctions, including morphological and functional thyroid involvement." | 1.35 | The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3,5,3'-triiodothyronine toxicosis of McCune-Albright syndrome. ( Brillante, BA; Celi, FS; Cherman, N; Chidakel, A; Collins, MT; Coppotelli, G; Feuillan, PP; Kelly, M; Shawker, T, 2008) |
| "We report a girl with McCune-Albright syndrome who presented with Cushing syndrome from adrenal hypersecretion and gonadotrophin-independent precocious puberty in the first year of life." | 1.30 | Occult T3 toxicosis in McCune-Albright syndrome. ( Brogan, P; Khadilkar, VV; Stanhope, R, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (33.33) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Hu, J | 1 |
| Hu, C | 1 |
| Roosimaa, M | 1 |
| Pajuväli, A | 1 |
| Peet, A | 1 |
| Tillmann, V | 1 |
| Pohlenz, J | 1 |
| Ahrens, W | 1 |
| Hiort, O | 1 |
| Celi, FS | 1 |
| Coppotelli, G | 1 |
| Chidakel, A | 1 |
| Kelly, M | 1 |
| Brillante, BA | 1 |
| Shawker, T | 2 |
| Cherman, N | 1 |
| Feuillan, PP | 2 |
| Collins, MT | 1 |
| Brogan, P | 1 |
| Khadilkar, VV | 1 |
| Stanhope, R | 1 |
| Rose, SR | 1 |
| Jones, J | 1 |
| Jeevanram, RK | 1 |
| Nisula, BC | 1 |
6 other studies available for triiodothyronine and Albright Syndrome
| Article | Year |
|---|---|
Postoperative thyroid crisis in an 11-year old male with McCune-Albright syndrome and atypical triiodothyronine hyperthyroidism: A case report.
Topics: Child; Femur; Fibrous Dysplasia, Polyostotic; Humans; Hyperthyroidism; Male; Postoperative Complicat | 2022 |
Low serum free thyroxine level in a girl with McCune-Albright syndrome.
Topics: Adolescent; Female; Fibrous Dysplasia, Polyostotic; Humans; Hyperthyroidism; Hypothyroidism; Thyroxi | 2015 |
A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy.
Topics: Calcium; Child; Erythrocyte Membrane; Fibrous Dysplasia, Polyostotic; Genotype; GTP-Binding Protein | 2003 |
The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3,5,3'-triiodothyronine toxicosis of McCune-Albright syndrome.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Algorithms; Cells, Cultured; Child; Child, Preschool; Ch | 2008 |
Occult T3 toxicosis in McCune-Albright syndrome.
Topics: Antithyroid Agents; Carbimazole; Child, Preschool; Female; Fibrous Dysplasia, Polyostotic; Humans; T | 1998 |
Thyroid abnormalities in the McCune-Albright syndrome: ultrasonography and hormonal studies.
Topics: Adolescent; Child; Child, Preschool; Female; Fibrous Dysplasia, Polyostotic; Humans; Thyroid Disease | 1990 |