Acromesomelic Dysplasia Syndrome

Overview of Acromesomelic Dysplasia Syndrome

Most recent studies have shown that Acromesomelic Dysplasia Syndrome shares some biological mechanisms with achondroplasia, apnea, bone-diseases-developmental, cytogenetic-abnormality, dislocations, dwarfism, dysplasia, grebe-syndrome, heart-failure, hereditary-diseases, hypertrophy, limb-deformities-congenital, mucopolysaccharidosis-iv, myopathy, osteoarthropathy, osteochondrodysplasias, skeletal-dysplasia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Acromesomelic Dysplasia Syndrome, and have been seen in publications frequently: Chondrocyte Proliferation, Endochondral Bone Growth, Excretion, Limb Morphogenesis, Localization, Phototransduction, Secretion, Segmentation, Transport

Quite a number of genes have been found to play important roles in Acromesomelic Dysplasia Syndrome, such as CNP, GDF5, GUCA2B, GUCY2C, GUCY2F, IGF1, NPR1, NPR2, NPR3, NPRL2, NPRL3, OSTN, OXA1L, STOM, STOML2. 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.

Acromesomelic Dysplasia Syndrome Related Genes

click to see detail information for each gene

Pathways Related to Acromesomelic Dysplasia Syndrome

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

Related Diseases