• Thumbnail for Multiple epiphyseal dysplasia
    Multiple epiphyseal dysplasia (MED), also known as Fairbank's disease, is a rare genetic disorder (dominant form: 1 in 10,000 births) that affects the...
    23 KB (2,399 words) - 04:17, 17 December 2023
  • Thumbnail for Autosomal recessive multiple epiphyseal dysplasia
    Autosomal recessive multiple epiphyseal dysplasia (ARMED), also called epiphyseal dysplasia, multiple, 4 (EDM4), multiple epiphyseal dysplasia with clubfoot...
    5 KB (425 words) - 03:47, 12 May 2024
  • Thumbnail for Pseudoachondroplasia
    also cause multiple epiphyseal dysplasia. Despite the radioclinical similarities between pseudoachondroplasia and multiple epiphyseal dysplasia, the latter...
    15 KB (1,695 words) - 20:51, 12 September 2024
  • Thumbnail for Legg–Calvé–Perthes disease
    hips are affected, should always be investigated to rule out multiple epiphyseal dysplasia. The condition is most commonly found in children between the...
    30 KB (3,816 words) - 11:47, 29 May 2024
  • Thumbnail for Wolcott–Rallison syndrome
    autosomal recessive disorder with infancy-onset diabetes mellitus, multiple epiphyseal dysplasia, osteopenia, mental retardation or developmental delay, and...
    9 KB (1,002 words) - 20:16, 1 December 2023
  • Thumbnail for Robert Reich
    women's clothing store. As a teenager, he was diagnosed with multiple epiphyseal dysplasia, also known as Fairbank's disease, a genetic disorder that results...
    61 KB (6,098 words) - 14:46, 5 October 2024
  • Thumbnail for David Wetherill
    table tennis player who has the rare bone development disorder Multiple Epiphyseal Dysplasia. Wetherill's hometown is Torpoint, Cornwall Wetherill completed...
    3 KB (247 words) - 23:03, 8 April 2024
  • Thumbnail for Megalencephaly
    responsible for the autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance". Orphanet Journal of Rare...
    23 KB (2,503 words) - 22:21, 7 September 2024
  • Thumbnail for Macrocephaly
    syndrome Multiple acyl-CoA dehydrogenase deficiency Multiple congenital anomalies-hypotonia-seizures syndrome Multiple epiphyseal dysplasia, Al-Gazali...
    18 KB (1,723 words) - 11:31, 16 September 2024
  • Thumbnail for Cartilage oligomeric matrix protein
    the osteochondrodysplasias pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED). COMP is a marker of cartilage turnover. It is present...
    11 KB (1,350 words) - 22:55, 18 January 2024