Congenital Pectus Carinatum

Overview of Congenital Pectus Carinatum

Most recent studies have shown that Congenital Pectus Carinatum shares some biological mechanisms with acquired-kyphosis, acquired-pectus-carinatum, bone-diseases-developmental, cicatrix, congenital-abnormality, congenital-funnel-chest, congenital-musculoskeletal-anomalies, depressive-disorder, dwarfism, dysplasia, hernia, hypoplasia, kyphoscoliosis-deformity-of-spine, osteochondrodysplasias, pain, poland-syndrome, protrusion, scoliosis-unspecified, thoracic-diseases.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Pectus Carinatum, and have been seen in publications frequently: Bone Resorption, Dehiscence, Endochondral Ossification, Excretion, Localization, Ossification, Pathogenesis, Regeneration, Swimming, Transport, Wound Healing

Quite a number of genes have been found to play important roles in Congenital Pectus Carinatum, such as ACAN, AMY2A, CBS, COL2A1, CTBP1, DCN, EFNB1, FEV, GALNS, GLB1, GUSB, NF1, PES1, TNFRSF11B, TNNT1, VPS13B. 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.

Congenital Pectus Carinatum Related Genes

click to see detail information for each gene

Pathways Related to Congenital Pectus Carinatum

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

Related Diseases