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triiodothyronine and Abnormalities, Multiple

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.

Research Excerpts

ExcerptRelevanceReference
"Craniofacial abnormalities including: microcephaly, underdeveloped maxilla, micrognathia, high arched palate, malocclusion, down-slanting palpebral fissures, thick eyelashes and full eyebrows."1.42Rubinstein-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."1.35Four 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."1.30Thyroid 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."1.27Hypothalamic-pituitary function in children with optic nerve hypoplasia. ( Costin, G; Murphree, AL, 1985)

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19905 (45.45)18.7374
1990's1 (9.09)18.2507
2000's2 (18.18)29.6817
2010's3 (27.27)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Langley, KG1
Trau, S1
Bean, LJ1
Narravula, A1
Schrier Vergano, SA1
Vlaeminck-Guillem, V1
Espiard, S1
Flamant, F1
Wémeau, JL1
Zwierzchowski, TJ1
Przedborska, A1
Wilmańska, I1
Raczkowski, JW1
Mussa, A1
Baldassarre, G1
Rosaia De Santis, L1
Gastaldi, R1
Corrias, A1
Silengo, MC1
HUTCHISON, JH1
ARNEIL, GC1
McGIRR, EM1
ZONDEK, H2
LESZYNSKY, HE2
ZONDEK, GW2
Frints, SG1
Lenzner, S1
Bauters, M1
Jensen, LR1
Van Esch, H1
des Portes, V1
Moog, U1
Macville, MV1
van Roozendaal, K1
Schrander-Stumpel, CT1
Tzschach, A1
Marynen, P1
Fryns, JP1
Hamel, B1
van Bokhoven, H1
Chelly, J1
Beldjord, C1
Turner, G1
Gecz, J1
Moraine, C1
Raynaud, M1
Ropers, HH1
Froyen, G1
Kuss, AW1
Tovar, JA1
Qi, B1
Diez-Pardo, JA1
Alfonso, LF1
Arnaiz, A1
Alvarez, FJ1
Valls-i-Soler, A1
Morreale de Escobar, G1
Costin, G1
Murphree, AL1
Götz, M1
Schenk, E1

Reviews

1 review available for triiodothyronine and Abnormalities, Multiple

ArticleYear
TRα receptor mutations extend the spectrum of syndromes of reduced sensitivity to thyroid hormone.
    Presse medicale (Paris, France : 1983), 2015, Volume: 44, Issue:11

    Topics: Abnormalities, Multiple; Adolescent; Adult; Age of Onset; Bradycardia; Child; Codon, Nonsense; Dwarf

2015

Other Studies

10 other studies available for triiodothyronine and Abnormalities, Multiple

ArticleYear
A 7-month-old male with Allan-Herndon-Dudley syndrome and the power of T3.
    American journal of medical genetics. Part A, 2015, Volume: 167A, Issue:5

    Topics: Abnormalities, Multiple; Humans; Infant; Intellectual Disability; Male; Mental Retardation, X-Linked

2015
Rubinstein-Taybi Syndrome in a 19-years old boy.
    Neuro endocrinology letters, 2015, Volume: 36, Issue:5

    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.
    Acta paediatrica (Oslo, Norway : 1992), 2008, Volume: 97, Issue:12

    Topics: Abnormalities, Multiple; Aortic Coarctation; Congenital Hypothyroidism; Cranial Fossa, Posterior; Ey

2008
Deficiency of an extra-thyroid enzyme in sporadic cretinism.
    Lancet (London, England), 1957, Aug-17, Volume: 273, Issue:6990

    Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Humans; Minerals; Syndrome; Thyroid (USP); Thyro

1957
Triac stosstherapy in sporadic goitrous cretinism.
    British medical journal, 1959, Feb-07, Volume: 1, Issue:5118

    Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Humans; Minerals; Syndrome; Triiodothyronine

1959
Triiodothyronine in myxedema and familial sporadic cretinism with goiter.
    Acta endocrinologica, 1955, Volume: 18, Issue:2

    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.
    European journal of human genetics : EJHG, 2008, Volume: 16, Issue:9

    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.
    Journal of pediatric surgery, 1997, Volume: 32, Issue:9

    Topics: Abnormalities, Drug-Induced; Abnormalities, Multiple; Animals; Disease Models, Animal; Female; Herni

1997
Hypothalamic-pituitary function in children with optic nerve hypoplasia.
    American journal of diseases of children (1960), 1985, Volume: 139, Issue:3

    Topics: Abnormalities, Multiple; Adolescent; Adrenocorticotropic Hormone; Adult; Child; Child, Preschool; Fe

1985
Weill-Marchesani syndrome. Growth hormone, thyroid and chromosome studies.
    Zeitschrift fur Kinderheilkunde, 1973, Dec-12, Volume: 116, Issue:1

    Topics: Abnormalities, Multiple; Body Constitution; Child; Eye Abnormalities; Fingers; Growth Hormone; Human

1973