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Hip dysplasia is a condition where the hip socket is too shallow to properly support the femoral head. It is often congenital and commonly detected during newborn screening examinations.
Hip dysplasia is a condition where the hip socket is too shallow to properly support the femoral head. It is often congenital and commonly detected during newborn screening examinations.
Hip dysplasia, also known as developmental dysplasia of the hip (DDH), is a condition in which the hip socket (acetabulum) is too shallow, too steep, or underdeveloped. As a result, the femoral head (the ball of the hip joint) is not properly covered and may slide partially or completely out of the socket – a condition known as hip dislocation (luxation). Hip dysplasia is one of the most common congenital musculoskeletal conditions and affects girls approximately four to five times more often than boys.
The exact causes of hip dysplasia are multifactorial. The following factors are known to increase the risk:
In newborns and infants, hip dysplasia is typically painless and may present with the following signs:
If left untreated, hip dysplasia can lead to pain, a limp, and early-onset hip osteoarthritis (coxarthrosis) in later childhood or adulthood.
Hip dysplasia is diagnosed through a combination of clinical and imaging methods:
Treatment depends on the severity of the dysplasia and the age of the patient. The goal is to centre the femoral head within the acetabulum and promote normal joint development.
When diagnosed early and treated consistently, the prognosis for hip dysplasia is generally excellent. Most affected children develop a normal, healthy hip joint. The later treatment begins, the more complex and prolonged the intervention – and the greater the risk of permanent joint damage or arthritis in adulthood.
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