triiodothyronine has been researched along with Abnormalities, Multiple in 11 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.
Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.
Excerpt | Relevance | Reference |
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"Craniofacial abnormalities including: microcephaly, underdeveloped maxilla, micrognathia, high arched palate, malocclusion, down-slanting palpebral fissures, thick eyelashes and full eyebrows." | 1.42 | Rubinstein-Taybi Syndrome in a 19-years old boy. ( Przedborska, A; Raczkowski, JW; Wilmańska, I; Zwierzchowski, TJ, 2015) |
"PHACES syndrome is a neurocutaneous condition characterized by the coexistence of large facial haemangiomas and at least one feature among posterior fossa malformations, cardiac and arterial anomalies, eye defects and sternal clefting." | 1.35 | Four new cases of PHACES syndrome: variable phenotypic expression and endocrine features. ( Baldassarre, G; Corrias, A; Gastaldi, R; Mussa, A; Rosaia De Santis, L; Silengo, MC, 2008) |
"Nitrofen treatment led to decreased plasma T3 and T4 levels without TSH changes." | 1.30 | Thyroid hormones in the pathogenesis of lung hypoplasia and immaturity induced in fetal rats by prenatal exposure to nitrofen. ( Alfonso, LF; Alvarez, FJ; Arnaiz, A; Diez-Pardo, JA; Morreale de Escobar, G; Qi, B; Tovar, JA; Valls-i-Soler, A, 1997) |
"Hypopituitarism was found in 15 patients." | 1.27 | Hypothalamic-pituitary function in children with optic nerve hypoplasia. ( Costin, G; Murphree, AL, 1985) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (45.45) | 18.7374 |
1990's | 1 (9.09) | 18.2507 |
2000's | 2 (18.18) | 29.6817 |
2010's | 3 (27.27) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Langley, KG | 1 |
Trau, S | 1 |
Bean, LJ | 1 |
Narravula, A | 1 |
Schrier Vergano, SA | 1 |
Vlaeminck-Guillem, V | 1 |
Espiard, S | 1 |
Flamant, F | 1 |
Wémeau, JL | 1 |
Zwierzchowski, TJ | 1 |
Przedborska, A | 1 |
Wilmańska, I | 1 |
Raczkowski, JW | 1 |
Mussa, A | 1 |
Baldassarre, G | 1 |
Rosaia De Santis, L | 1 |
Gastaldi, R | 1 |
Corrias, A | 1 |
Silengo, MC | 1 |
HUTCHISON, JH | 1 |
ARNEIL, GC | 1 |
McGIRR, EM | 1 |
ZONDEK, H | 2 |
LESZYNSKY, HE | 2 |
ZONDEK, GW | 2 |
Frints, SG | 1 |
Lenzner, S | 1 |
Bauters, M | 1 |
Jensen, LR | 1 |
Van Esch, H | 1 |
des Portes, V | 1 |
Moog, U | 1 |
Macville, MV | 1 |
van Roozendaal, K | 1 |
Schrander-Stumpel, CT | 1 |
Tzschach, A | 1 |
Marynen, P | 1 |
Fryns, JP | 1 |
Hamel, B | 1 |
van Bokhoven, H | 1 |
Chelly, J | 1 |
Beldjord, C | 1 |
Turner, G | 1 |
Gecz, J | 1 |
Moraine, C | 1 |
Raynaud, M | 1 |
Ropers, HH | 1 |
Froyen, G | 1 |
Kuss, AW | 1 |
Tovar, JA | 1 |
Qi, B | 1 |
Diez-Pardo, JA | 1 |
Alfonso, LF | 1 |
Arnaiz, A | 1 |
Alvarez, FJ | 1 |
Valls-i-Soler, A | 1 |
Morreale de Escobar, G | 1 |
Costin, G | 1 |
Murphree, AL | 1 |
Götz, M | 1 |
Schenk, E | 1 |
1 review available for triiodothyronine and Abnormalities, Multiple
Article | Year |
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TRα receptor mutations extend the spectrum of syndromes of reduced sensitivity to thyroid hormone.
Topics: Abnormalities, Multiple; Adolescent; Adult; Age of Onset; Bradycardia; Child; Codon, Nonsense; Dwarf | 2015 |
10 other studies available for triiodothyronine and Abnormalities, Multiple
Article | Year |
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A 7-month-old male with Allan-Herndon-Dudley syndrome and the power of T3.
Topics: Abnormalities, Multiple; Humans; Infant; Intellectual Disability; Male; Mental Retardation, X-Linked | 2015 |
Rubinstein-Taybi Syndrome in a 19-years old boy.
Topics: Abnormalities, Multiple; Craniofacial Abnormalities; CREB-Binding Protein; Foot Deformities; Hand De | 2015 |
Four new cases of PHACES syndrome: variable phenotypic expression and endocrine features.
Topics: Abnormalities, Multiple; Aortic Coarctation; Congenital Hypothyroidism; Cranial Fossa, Posterior; Ey | 2008 |
Deficiency of an extra-thyroid enzyme in sporadic cretinism.
Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Humans; Minerals; Syndrome; Thyroid (USP); Thyro | 1957 |
Triac stosstherapy in sporadic goitrous cretinism.
Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Humans; Minerals; Syndrome; Triiodothyronine | 1959 |
Triiodothyronine in myxedema and familial sporadic cretinism with goiter.
Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Goiter; Humans; Minerals; Myxedema; Syndrome; Th | 1955 |
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression.
Topics: Abnormalities, Multiple; Adolescent; Adult; Child, Preschool; Chromosomes, Human, Pair 9; Chromosome | 2008 |
Thyroid hormones in the pathogenesis of lung hypoplasia and immaturity induced in fetal rats by prenatal exposure to nitrofen.
Topics: Abnormalities, Drug-Induced; Abnormalities, Multiple; Animals; Disease Models, Animal; Female; Herni | 1997 |
Hypothalamic-pituitary function in children with optic nerve hypoplasia.
Topics: Abnormalities, Multiple; Adolescent; Adrenocorticotropic Hormone; Adult; Child; Child, Preschool; Fe | 1985 |
Weill-Marchesani syndrome. Growth hormone, thyroid and chromosome studies.
Topics: Abnormalities, Multiple; Body Constitution; Child; Eye Abnormalities; Fingers; Growth Hormone; Human | 1973 |