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Disease Info Card
Congenital Myotonic Dystrophy
Information about Congenital Myotonic Dystrophy: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Congenital Myotonic Dystrophy
Most recent studies have shown that Congenital Myotonic Dystrophy shares some biological mechanisms with atrophy, congenital-clubfoot, congenital-structural-myopathy, coronary-microvascular-disease, dystrophy, muscle-hypotonia, muscle-weakness, muscular-dystrophy, myopathy, myotonia-congenita, myotonic-dystrophy, neuromuscular-diseases, pathological-dilatation, polyhydramnios, pregnancy-complications, respiratory-distress, trinucleotide-repeat-expansion, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Myotonic Dystrophy, and have been seen in publications frequently: Aging, Autophagy, Cardiac Conduction, Cognition, Dna Methylation, Fertilization, Gastric Emptying, Gastric Motility, Localization, Methylation, Mrna Splicing, Muscle Atrophy, Muscle Hypertrophy, Myelination, Pathogenesis
Quite a number of genes have been found to play important roles in Congenital Myotonic Dystrophy, such as ACTA1, ATG5, BCAP31, BIN1, CALD1, CP, DMPK, DNM2, EPO, FDXR, GRIP1, MBNL1, MRPL28, MTM1, PRL, RYR1, SIX5, TPM3, UTRN. 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.