Langer Mesomelic Dysplasia Syndrome

Overview of Langer Mesomelic Dysplasia Syndrome

Most recent studies have shown that Langer Mesomelic Dysplasia Syndrome shares some biological mechanisms with bone-diseases-developmental, congenital-abnormality, congenital-musculoskeletal-anomalies, dwarfism, dysplasia, growth-disorders, growth-retardation, haploinsufficiency, hypoplasia-of-scrotum, leri-weill-dyschondrosteosis, limb-deformities-congenital, madelungs-deformity, micrognathism, osteochondrodysplasias, skeletal-dysplasia, turner-syndrome.

Among the many pathways, these few ones have gauged particular interests from scientists studying Langer Mesomelic Dysplasia Syndrome, and have been seen in publications frequently: Bone Development, Chondrocyte Hypertrophy, Chondrocyte Proliferation, Endochondral Ossification, Limb Development, Localization, Meiosis, Meiosis I, Ossification, Pathogenesis

Quite a number of genes have been found to play important roles in Langer Mesomelic Dysplasia Syndrome, such as BMP4, CHP1, COMP, DCTN3, DYNC1H1, F2R, FGFR3, FMN1, GGH, GH1, IHH, NR1I2, PHB2, RUNX2, RUNX3, SHOX, SHOX2, SLC52A2, SOX3. 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.

Langer Mesomelic Dysplasia Syndrome Related Genes

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Pathways Related to Langer Mesomelic Dysplasia Syndrome

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

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