RECESSIVE MULTIPLE EPIPHYSEAL DYSPLASIA: A CASE REPORT

Main Article Content

Saeed Bin Ayaz
Samia Rauf
Fatima Ayaz

Abstract

Multiple epiphyseal dysplasia (MED) is characterized by abnormal bone and cartilage development particularly affecting epiphysis of long bones. Individuals with MED present during childhood presents with hip pain, knee pain and waddling gait. The autosomal recessive MED is differentiated from the dominant type by the presence of hands, knees and feet malformations with scoliosis. We present here, a case of autosomal recessive MED, an eleven and half years old boy who presented with pain in knees, difficulty walking, abnormal fingers and abnormal toes. The radiographs of hands, knees and pelvis were suggestive of an abnormal epiphyseal development. After diagnosis, patient was counseled and he was advised analgesics and different exercises.

Article Details

How to Cite
Ayaz, S. B., S. Rauf, and F. Ayaz. “RECESSIVE MULTIPLE EPIPHYSEAL DYSPLASIA: A CASE REPORT”. KHYBER MEDICAL UNIVERSITY JOURNAL, vol. 11, no. 2, June 2019, pp. 104-6, doi:10.35845/kmuj.2019.18338.
Section
Case Report
Author Biographies

Saeed Bin Ayaz, Combined Military Hospital Quetta and Quetta Institute of Medical Sciences, Quetta

Consultant and Head of the Department of Rehabilitation Medicine

Samia Rauf, Department of Diagnostic Radiology, Combined Military Hospital Quetta and Quetta institute of Medical Sciences, Quetta 87300, Balochistan, Pakistan

COnsultant

Fatima Ayaz, Registrar Internal Medicine, Holy Family Hospital, Rawalpindi, Pakistan.

Registrar Internal Medicine

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