Multiple Pterygium Syndrome

Overview of Multiple Pterygium Syndrome

Most recent studies have shown that Multiple Pterygium Syndrome shares some biological mechanisms with arthrogryposis, cleft-lip, cleft-palate, congenital-abnormality, congenital-foot-deformity, congenital-webbing, edema, fetal-death, flexed-fetal-attitude, hypoplasia, lymphangioma-cystic, multiple-pterygium-syndrome-lethal-type, muscle-contracture, popliteal-pterygium-syndrome, pterygium, scoliosis-unspecified, skin-abnormalities, syndactyly, van-der-woude-syndrome.

Among the many pathways, these few ones have gauged particular interests from scientists studying Multiple Pterygium Syndrome, and have been seen in publications frequently: Cell Cycle, Fertilization, Gastrulation, Keratinocyte Differentiation, Limb Development, Localization, Muscle Contraction, Pathogenesis, Somite Development, Transposition

Quite a number of genes have been found to play important roles in Multiple Pterygium Syndrome, such as CHRNA1, CHRND, CHRNG, CHUK, DOK7, FLAD1, INPP5K, IRF6, PEX7, RAPSN, REXO2, RIPK4, SFN, THBD, TNIP1, TPM2, TWIST1. 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.

Multiple Pterygium Syndrome Related Genes

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Pathways Related to Multiple Pterygium Syndrome

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

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