Distal Arthrogryposis Syndrome

Overview of Distal Arthrogryposis Syndrome

Most recent studies have shown that Distal Arthrogryposis Syndrome shares some biological mechanisms with arthrogryposis, arthrogryposis-distal-type-2b, arthrogryposis-multiplex-congenita, blepharoptosis, cleft-palate, congenital-abnormality, congenital-camptodactyly, congenital-clubfoot, congenital-foot-deformity, congenital-hand-deformities, dwarfism, flexed-fetal-attitude, freeman-sheldon-syndrome, muscle-contracture, muscle-weakness, myopathy, ophthalmoplegia, scoliosis-unspecified, weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Distal Arthrogryposis Syndrome, and have been seen in publications frequently: Dehiscence, Localization, Melanocyte Migration, Metaphase, Muscle Contraction, Ossification, Pathogenesis, Regulation Of Muscle Contraction, Secretion

Quite a number of genes have been found to play important roles in Distal Arthrogryposis Syndrome, such as ACTA1, ATRX, FBN2, MYBPC1, MYH14, MYH2, MYH3, MYH7, MYH8, NEB, PFDN4, THBD, TNNI2, TNNT1, TNNT3, TPM2. 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.

Distal Arthrogryposis Syndrome Related Genes

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Pathways Related to Distal Arthrogryposis Syndrome

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

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