adrenic acid has been researched along with Chondrodysplasia Punctata in 1 studies
adrenic acid: RN given refers to cpd without isomeric designation
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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Christensen, E | 1 |
| Grønn, M | 1 |
| Hagve, TA | 1 |
| Kase, BF | 1 |
| Christophersen, BO | 1 |
1 other study available for adrenic acid and Chondrodysplasia Punctata
| Article | Year |
|---|---|
Adrenoleukodystrophy. The chain shortening of erucic acid (22:1(n-9)) and adrenic acid (22:4(n-6)) is deficient in neonatal adrenoleukodystrophy and normal in X-linked adrenoleukodistrophy skin fibroblasts.
Topics: Adrenoleukodystrophy; Arachidonic Acid; Arachidonic Acids; Cells, Cultured; Chondrodysplasia Punctat | 1989 |