Langer-giedion Syndrome

Overview of Langer-giedion Syndrome

Most recent studies have shown that Langer-giedion Syndrome shares some biological mechanisms with cartilaginous-exostosis, chromosome-8-deletion, cleft-palate, congenital-abnormality, congenital-hand-deformities, cytogenetic-abnormality, dwarfism, dysplasia, exostoses, hair-diseases, hereditary-multiple-exostoses, hypotrichosis, microcephaly, neoplasms, nephroblastoma, prader-willi-syndrome, trichorhinophalangeal-dysplasia-type-i.

Among the many pathways, these few ones have gauged particular interests from scientists studying Langer-giedion Syndrome, and have been seen in publications frequently: Bone Development, Cell Proliferation, Chromosome Breakage, Limb Development, Localization, Metaphase, Mitotic Recombination, Pathogenesis, Translation

Quite a number of genes have been found to play important roles in Langer-giedion Syndrome, such as BCL9, BMP1, CDKN2B, EIF3H, EXT1, EXT2, INVS, LMLN, MB, MRPL28, MYC, NXT1, PAX6, POLD4, SUB1, TBPL1, TRPS1, TYRP1, WT1. 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-giedion Syndrome Related Genes

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Pathways Related to Langer-giedion Syndrome

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

Related Diseases