Hip dysplasia, developmental dysplasia of the hip (DDH) or congenital dysplasia of the hip (CDH) is a congenital or acquired deformation or misalignment of the hip joint.
The use of the word congenital can also imply that the condition already exists at birth. This terminology introduces challenges, because the joint in a newborn is formed from cartilage and still malleable, making the onset difficult to ascertain.
The newer term DDH also encompasses occult dysplasia (e.g. an underdeveloped joint) without dislocation and dislocation developing after the "newborn" phase.
The term is not used consistently. In pediatric/neonatal orthopedics it is used to describe unstable/dislocatable hips and poorly developed acetabula. For adults it describes hips showing abnormal femur head or acetabular x-rays.
Some sources prefer the term "hip dysplasia" over DDH, considering it to be "simpler and more accurate", partly because of the redunancy created by the use of the terms developmental and dysplasia.
Hip dysplasia can range from barely detectable to severely malformed / dislocated. The congenital form, teratologic or non-reducible dislocation occurs as part of more complex conditions.
The condition can be bilateral or unilateral:
If the joint is fully dislocated a false acetabulum often forms (often higher up on the pelvis) opposite the dislocated femoral head position.
In actetabular dysplasia the acetabulum (socket) is too shallow or deformed. The center-edge angle is measured as described by Wiberg . In coxa vara the femur head grows at too narrow an angle to the shaft, in coxa valga the angle is too wide.
A rare type, the "Beukes familial hip dysplasia" is found among Afrikaners that are members of the Beukes family. The femur head is flat and irregular. Sufferers develop osteoarthritis at an early age.
In 1979 Dr. John F. Crowe et al proposed a classification to define the degree of malformation and dislocation. Grouped from least severe Crowe I dysplasia to most severe Crowe IV. This classification is very useful for studying treatment results.
Rather than using the Wiberg angle because it makes it difficult to quantify the degree of dislocation they used 3 key elements to determine the degree of subluxation: A reference line at the lower rim of the "teardrop", junction between the femoral head and neck of the respective joint and the height of the pelvis (vertical measurement). They studied anteroposterior pelvic x-rays and drew horizontal lines through the lower rim of a feature called "teardrop". The distance between this line and the middle lines of the junction between femur head and neck gave them a measure of the degree of femur head subluxation. They further established that a "normal" diameter of the femur head measures 20% of the hight of the pelvis. If the middle line of the neck-head junction was more than 10% of the pelvis hight above the reference line they considered the joint to be more than 50% dislocated.
The following types resulted:
| Class | Description | Dislocation |
| Crowe I | Femur and acetabulum show minimal abnormal development. | Less than 50% dislocation |
| Crowe II | The acetabulum shows abnormal development. | 50% to 75% dislocation |
| Crowe III | The acetabula is developed without a roof. A false acetabulum develops opposite the dislocated femur head position. The joint is fully dislocated. | 75% to 100% dislocation |
| Crowe IV | The acetabulum is insufficiently developed. Since the femur is positioned high up on the pelvis this class is also known as "high hip dislocation". | More than 100% dislocation |
An instability rate of 1:60 has been described, though this rate drops to 1:240 at one week. The condition occurs with higher frequency in females than in males.
Hip dysplasia is considered to be a multifactorial condition: that means that several factors are involved in causing the condition to manifest.
Some studies suggest a hormonal link. Specifically the hormone relaxin has been indicated.
A genetic factor is indicated by the trait running in families and increased occurrence in some ethnic populations (e.g. native Americans, Lapps / Sami people). A locus has been described on chromosome 13. Beukes familial dysplasia, on the other hand, was found to map to an 11-cM region on chromosome 4q35. With nonpenetrant carriers not affected.
Further risk factors include breech birth and firstborns. In breech position the femoral head tends to get pushed out of the socket. A narrow uterus also facilitates hip joint dislocation during fetal development and birth.
The condition can be confirmed by ultrasound and X-ray. Ultrasound imaging yields better results defining the anatomy until the cartilage is ossified. When the infant is around 3 months old a clear roentgenographic image can be achieved. Unfortunately the time the joint gives a good x-ray image is also is the point at which nonsurgical treatment methods cease to give good results. In x-ray imaging dislocation may be indicated if the Shenton's line (an arc drawn from the medial femoral neck through the superior margin of the obturator foramen) does not result in a smooth arc.
Asymmetrical gluteal folds and an apparent limb-length inequality can further indicate unilateral hip dysplasia. Most vexingly, many newborn hips show a certain ligamentous laxity, which can make severely malformed joints appear stable. That is one reason why follow-up exams and developmental monitoring are important. Routine ultrasound screening has been discussed and rejected mainly because the small benefit would not justify the costs.
The Harris hip score (developed by William H. Harris MD, an orthopedist from Massachusetts) is one way to evaluate hip function following surgery. Other scoring methods are based on patients' evaluation like e.g. the Oxford hip score, HOOS and WOMAC score. Children's Hospital Oakland Hip Evaluation Scale (CHOHES) is a modification of the Harris hip score that is currently being evaluated.
Other devices employed include the spica cast, particularly following surgical closed reduction. A few weeks in traction can be used as part of a treatment plan.
Osteotomies are either used in conjunction with arthroplasty or by themselves to correct misalignment.
In the television program "ER," Kerry Weaver uses a crutch owing to congenital hip dysplasia. In season 12, she undergoes a hip replacement to cure her dysplasia when her previously untreated joint worsens.



