{Reference Type}: Case Reports
{Title}: Spondyloepiphyseal Dysplasia Tarda with Progressive Arthropathy Associated with Early-onset Hip Arthritis - A Case Report.
{Author}: Prabaharan C;Harshavardhan JKG;Menon PG;
{Journal}: J Orthop Case Rep
{Volume}: 11
{Issue}: 1
{Year}: 2021
暂无{DOI}: 10.13107/jocr.2021.v11.i01.1986
{Abstract}: <B>UNASSIGNED: </B>Spondyloepiphyseal dysplasia tarda with progressive arthropathy (SEDT-PA) is a rare inherited dysfunction with autosomal recessive inheritance. SEDT-PA is also named as progressive pseudorheumatoid arthropathy of childhood as it is associated with multiple joint contractures and arthritis. We report a case of SEDT-PA managed with bilateral stage total hip arthroplasty.<BR><B>UNASSIGNED: </B>A 22-year-old lady presented with severe bilateral hip arthritis. Based on her clinical and radiological features described in this article, she was diagnosed as having SEDT-PA. She was managed with bilateral stage total hip arthroplasty. The pre-operative planning and technical challenges of performing this procedure have been described.<BR><B>UNASSIGNED: </B>Dysfunctions originally of genetic origin like spondyloepiphyseal dysplasia tarda mimics and is commonly misdiagnosed as juvenile chronic arthritis. These patients have disabling early-onset hip arthritis which requires surgery. Arthroplasty is challenging in these patients because of the low proximal femur offset but good results can be obtained after thorough pre-operative planning to tackle intraoperative difficulties.