23 top medical experts on 5 multiple Epiphyseal dysplasia across 2 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- 5 multiple Epiphyseal dysplasia: Multiple epiphyseal dysplasia type 5 is a multiple epiphyseal dysplasia characterized by an early-onset of pain and stiffness (involving knee and hip), progressive deformity of the extremities and precocious osteoarthritis associated with delayed and irregular ossification of epiphyses. Features specific to multiple epiphyseal dysplasia, type 5 include normal stature and lesser incidence of gait abnormalities. Radiographs reveal epiphyseal and metaphyseal irregularities. Multiple epiphyseal dysplasia type 5 follows an autosomal dominant mode of transmission.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Bilateral Hereditary Microepiphyseal Dysplasia, Matn3-Related Multiple Epiphyseal Dysplasia, Multiple epiphyseal dysplasia 5, MATN3 related Multiple epiphyseal dysplasia
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