Page last updated: 2024-09-27
Developmental Dysplasia of the Hip
Dislocation of the HIP JOINT from an abnormal FEMORAL HEAD to the ACETABULUM relationship. It is most often due to ligamentous laxity, abnormal positioning of the joint and various other developmental, congenital factors, and method of delivery (e.g., OLIGOHYDRAMNIOS). When dislocation is diagnosed in neonates it is referred to as CONGENITAL HIP DYSPLASIA.
Synonyms(4)
| Synonym |
|---|
| Developmental Dysplasia of the Hip |
| Developmental Hip Dislocation |
| Developmental Hip Dysplasia |
| Hip Dislocation, Developmental |
Research Excerpts
Treatment
Research
Studies (9)
| Timeframe | Studies, This Condition (%) | All Conditions % |
|---|
| pre-1990 | 0 (0.00) | 23.3326 |
| 1990's | 0 (0.00) | 12.5806 |
| 2000's | 0 (0.00) | 18.1394 |
| 2010's | 0 (0.00) | 28.8240 |
| 2020's | 9 (100.00) | 9.53 |
Protein Targets (20)
| Protein | Potency Measurements | Inhibition Measurements | Activation Measurements | Drugs |
|---|
| Chain A, Integrase | 0 | 1 | 0 | 1 |
| Chain A, Integrase | 0 | 1 | 0 | 1 |
| Chain A, T4 LYSOZYME | 0 | 0 | 1 | 1 |
| Chain A, GCN4P1 | 0 | 0 | 1 | 1 |
| Chain B, GCN4P1 | 0 | 0 | 1 | 1 |
| Chain C, GCN4P1 | 0 | 0 | 1 | 1 |
| Chain A, T4 LYSOZYME | 0 | 0 | 1 | 1 |
| Chain A, T4 LYSOZYME | 0 | 0 | 1 | 1 |
| Chain A, Replicase polyprotein 1ab | 0 | 1 | 0 | 1 |
| Chain A, 3C-like proteinase | 0 | 1 | 0 | 1 |
| pregnane X receptor | 1 | 0 | 0 | 1 |
| thyroid stimulating hormone receptor | 1 | 0 | 0 | 1 |
| progesterone receptor | 1 | 0 | 0 | 1 |
| retinoid X nuclear receptor alpha | 1 | 0 | 0 | 1 |
| peroxisome proliferator-activated receptor delta | 1 | 0 | 0 | 1 |
| cellular tumor antigen p53 isoform a | 1 | 0 | 0 | 1 |
| Endolysin | 0 | 0 | 1 | 1 |
| Cellular tumor antigen p53 | 1 | 0 | 0 | 1 |
| Integrin beta-3 | 1 | 0 | 0 | 1 |
| Integrin alpha-IIb | 1 | 0 | 0 | 1 |
| [prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |