Page last updated: 2024-10-18

iodine and Chondrodysplasia Punctata

iodine has been researched along with Chondrodysplasia Punctata in 1 studies

Iodine: A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
diiodine : Molecule comprising two covalently bonded iodine atoms with overall zero charge..

Chondrodysplasia Punctata: A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC), an autosomal dominant form (Conradi-Hunermann syndrome), and a milder X-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Refetoff, S1
DeWind, LT1
DeGroot, LJ1

Other Studies

1 other study available for iodine and Chondrodysplasia Punctata

ArticleYear
Familial syndrome combining deaf-mutism, stuppled epiphyses, goiter and abnormally high PBI: possible target organ refractoriness to thyroid hormone.
    The Journal of clinical endocrinology and metabolism, 1967, Volume: 27, Issue:2

    Topics: Child; Child, Preschool; Chondrodysplasia Punctata; Deafness; Female; Goiter; Heart Rate; Humans; In

1967