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triiodothyronine and Eye Abnormalities

triiodothyronine has been researched along with Eye Abnormalities in 2 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.

Eye Abnormalities: Congenital absence of or defects in structures of the eye; may also be hereditary.

Research Excerpts

ExcerptRelevanceReference
"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)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mussa, A1
Baldassarre, G1
Rosaia De Santis, L1
Gastaldi, R1
Corrias, A1
Silengo, MC1
Götz, M1
Schenk, E1

Other Studies

2 other studies available for triiodothyronine and Eye Abnormalities

ArticleYear
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
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