9 top medical experts on 4 multiple Epiphyseal dysplasia across 0 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 4 multiple Epiphyseal dysplasia: Multiple epiphyseal dysplasia type 4 is a multiple epiphyseal dysplasia with a late-childhood onset, characterized by joint pain involving hips, knees, wrists, and fingers with occasional limitation of joint movements, deformity of hands, feet, and knees (club foot, clinodactyly, brachydactyly), scoliosis and slightly reduced adult height. Radiographs display flat epiphyses with early arthritis of the hip, and double-layered patella. Multiple epiphyseal dysplasia type 4 follows an autosomal recessive mode of transmission. The disease is allelic to diastrophic dwarfism, atelosteogenesis type 2 and achondrogenesis type 1B with whom it forms a clinical continuum.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Autosomal recessive multiple epiphyseal dysplasia,  Multiple epiphyseal dysplasia 4,  Multiple epiphyseal dysplasia with bilayered patellae,  Multiple epiphyseal dysplasia with clubfoot,  Multiple epiphyseal dysplasia with double-layered patella,  autosomal recessive Multiple epiphyseal dysplasia


  

        

                    


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