Some hips are anatomically different from birth or have been significantly altered by disease. Developmental dysplasia of the hip (DDH) results in a shallow socket that leads to premature wear, while sickle-cell disease can compromise blood supply to the femoral head. Such cases require a surgeon who carefully plans around the unusual anatomy — rather than merely operating through it.

If you recognize two or more of these symptoms, a professional assessment is your best next step.
In cases of DDH and sickle-cell hip disease, surgical timing is a matter of strategy: operating too early can compromise the implant's lifespan, while delaying too long causes the bone stock to deteriorate. The optimal time is when pain significantly limits your daily life and imaging confirms disease progression — at this point, a carefully planned reconstruction can restore the function that your anatomy never naturally provided.
Dr. Mohammed Ali Balhareth — consultant orthopedic surgeon specializing in hip & knee replacement, reconstruction, and trauma surgery in Riyadh.
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