Dislocation of hip
Dislocation of hip
Classification & external resources
| ICD-10 |
S73.0, Q65.0-Q65.2 |
| ICD-9 |
835 |
| OMIM |
142700 |
| DiseasesDB |
3056 |
| eMedicine |
emerg/144 |
| MeSH |
D006618 |
A dislocated hip is a condition that can be congenital or acquired. Congenital hip dislocations are much more common in girls than in boys.
Posterior vs. anterior
Nine out of ten hip dislocations are posterior. The affected limb will be shortened and internally rotated in this case.
In an anterior dislocation the limb will not be lengthened as noticeably and will be externally rotated.
Congenital vs. acquired
Congenital hip dislocation must be detected early when it can be easily treated by a few weeks of traction. If it is not detected, the child's hip may develop incorrectly seen when the child begins to walk. If one hip is affected the child will be have a limp and lurch and with bilateral dislocation there will be a waddling gait. On physical exam, with the baby in the supine position, the examiner flexes the hips and knees both to 90 degrees, and, holding the knees, pushes gently downward, which may induce a posterior dislocation or subluxation. Keeping the baby in this 90 degree flexed position, the examiner then externally rotates the thighs. A normal infant will demonstrate no evidence of dislocation. Congenital hip dislocation is much more common in girls than boys.
Acquired hip dislocations can be extremely painful and commonly occur during car accidents. They may be treated by surgical realignment and traction.
See also
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Congenital malformations and deformations of musculoskeletal system (Q65-Q79, 754-756) |
| Limbs |
hip: Dislocation of hip/Hip dysplasia
feet (Club foot, Flat feet, Pes cavus)
head, face, spine and chest: skull, face and jaw (Dolichocephaly, Plagiocephaly) - Scoliosis - chest (Pectus excavatum, Pectus carinatum)
Polydactyly/Syndactyly (Webbed toes)
reduction deficits (Ectrodactyly, Amelia, Phocomelia)
upper limb (Cleidocranial dysostosis, Madelung's deformity, Sprengel's deformity)
knee (Genu valgum, Genu varum)
Arthrogryposis |
| Skull and face bones |
Craniosynostosis (Scaphocephaly) - Trigonocephaly - Oxycephaly - Crouzon syndrome - Hypertelorism - Macrocephaly - Treacher Collins syndrome - Platybasia |
| Spine and bony thorax |
Klippel-Feil syndrome - Spondylolisthesis - Cervical rib - Bifid rib |
| Osteochondrodysplasia |
growth of tubular bones and spine: Achondrogenesis - Thanatophoric dysplasia - Short rib-polydactyly syndrome - Chondrodysplasia punctata (Rhizomelic chondrodysplasia punctata, Conradi-Hünermann syndrome), Achondroplasia (Hypochondroplasia, Osteosclerosis congenita) - Ellis-van Creveld syndrome - Spondyloepiphyseal dysplasia congenita
Osteogenesis imperfecta - McCune-Albright syndrome - Osteopetrosis - Metaphyseal dysplasia - Hereditary multiple exostoses - Osteopoikilosis - Chondrodystrophy - Osteodystrophy |
| Other |
abdominal wall (Congenital diaphragmatic hernia, Omphalocele, Gastroschisis, Prune belly syndrome) - Ehlers-Danlos syndrome |
| See also non-congenital conditions (M, 710-739) |
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