Madelung's Deformity

Overview of Madelung's Deformity

Most recent studies have shown that Madelung's Deformity shares some biological mechanisms with arthropathy, bone-diseases-developmental, congenital-abnormality, congenital-hand-deformities, dislocations, dwarfism, dysplasia, epiphysis-disorders, fracture, growth-disorders, haploinsufficiency, langer-mesomelic-dysplasia-syndrome, leri-weill-dyschondrosteosis, osteochondrodysplasias, pain, skeletal-dysplasia, subluxation-of-joint, turner-syndrome.

Among the many pathways, these few ones have gauged particular interests from scientists studying Madelung's Deformity, and have been seen in publications frequently: Bone Maturation, Endochondral Ossification, Limb Development, Localization, Male Meiosis, Meiosis, Menarche, Metaphase, Methylation, Ossification, Pathogenesis, Reflex, Translation

Quite a number of genes have been found to play important roles in Madelung's Deformity, such as CACNA1C, CHP1, DCTN3, DYNC1H1, F2R, GGH, GH1, GRIP1, MAOA, NR1I2, PHB2, SHOX, SLC52A2, STS, TBXAS1, TYMS. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Madelung's Deformity Related Genes

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Pathways Related to Madelung's Deformity

This information is being compiled and will come in a future update

Related Diseases