Weill-marchesani Syndrome

Overview of Weill-marchesani Syndrome

Most recent studies have shown that Weill-marchesani Syndrome shares some biological mechanisms with angle-closure-glaucoma, brachydactyly, congenital-ectopia, connective-tissue-diseases, disorder-of-eye, dwarfism, ectopia-lentis, eye-abnormalities, glaucoma, growth-disorders, intraocular-pressure-disorder, joint-stiffness, lens-subluxation, marfan-syndrome, myopia, secondary-glaucoma, severe-myopia, spherophakia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Weill-marchesani Syndrome, and have been seen in publications frequently: Angiogenesis, Cell Adhesion, Dehiscence, Heart Development, Localization, Muscle Hypertrophy, Pathogenesis, Protein Folding, Protein Processing, Rna Splicing, Secretion, Signal Peptide Processing, Translation

Quite a number of genes have been found to play important roles in Weill-marchesani Syndrome, such as ADAMTS1, ADAMTS10, ADAMTS17, ADAMTSL2, ADAMTSL4, AKR1B1, AR, AREG, CAT, FBN1, FBN2, FBN3, FDXR, LTBP1, LTBP2, LTBP3, MID1, PAEP, TNF. 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.

Weill-marchesani Syndrome Related Genes

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Pathways Related to Weill-marchesani Syndrome

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

Related Diseases