2024年12月30日 · Multiple epiphyseal dysplasia (MED), also known as dysplasia epiphysealis multiplex or Fairbank disease, refers to a group of skeletal dysplasias characterized by disorganized enchondral epiphyseal ossification in the long bones.

Multiple epiphyseal dysplasia is a skeletal dysplasia characterized by disorganized enchondral epiphyseal ossification in the long bones. The disease usually presents with articular pain, mostly in weight-bearing joints.

Multiple epiphyseal dysplasia (MED) is a rare genetic disorder (an autosomal dominant pattern) that affects the growing ends of bones, characterized by flattening and fragmentation of epiphyses.

Alkhateeb K, Multiple epiphyseal dysplasia. Case study, Radiopaedia.org (Accessed on 23 Aug 2024) https://doi.org/10.53347/rID-86496

Multiple epiphyseal dysplasia also known as dysplasia epiphyseal multiplex or Fairbank disease) is inherited in an autosomal dominant pattern characterised by flattening and fragmentation of epiphyses.

2022年3月29日 · Spondyloepiphyseal dysplasia is a form of skeletal dysplasia mainly involving the spine and proximal epiphyses.

2024年8月20日 · polydactyly with skeletal dysplasia usually indicates short rib polydactyly syndrome, chondrodysplasia punctata, or asphyxiating thoracic dysplasia. Treatment and prognosis. The prognosis is widely variable, ranging from being lethal to very mild cosmetic deficits. See also. lethal skeletal dysplasias

2020年10月10日 · - “ Irregular and delayed ossification of multiple epiphyses with associated genu valgus in a patient with three of the siblings have the same anomali...” Used in the following article: Multiple epiphyseal dysplasia

2021年1月18日 · Meyer dysplasia (also known as dysplasia epiphysealis capitis femoris) is a fragmentation and delayed ossification of the femoral capital epiphyses that affects the pediatric hips. It is considered more of a normal hip developmental variation rather than a true dysplasia.

2023年6月4日 · Dysplasia epiphysealis hemimelica (DEH), also known as Trevor disease, is an extremely rare, non-hereditary disease that is characterized by osteochondromas arising from the epiphyses.