Disease Info Card

Klippel-feil Syndrome

Information about Klippel-feil Syndrome: 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 Klippel-feil Syndrome

Most recent studies have shown that Klippel-feil Syndrome shares some biological mechanisms with arnold-chiari-malformation, cleft-palate, complete-hearing-loss, compression-of-spinal-cord, conductive-hearing-loss, congenital-abnormal-synostosis, congenital-abnormality, congenital-absence, congenital-elevation-of-scapula, duane-retraction-syndrome, dysplasia, hydrocephalus, ophthalmoplegia, pain, platybasia, scoliosis-unspecified, spina-bifida, spinal-cord-diseases, spinal-diseases, wildervancks-syndrome.

Among the many pathways, these few ones have gauged particular interests from scientists studying Klippel-feil Syndrome, and have been seen in publications frequently: Axon Guidance, Dehiscence, Developmental Process, Embryo Development, Embryonic Morphogenesis, Endochondral Ossification, Enucleation, Gastrulation, Hormone Secretion, Localization, Neural Tube Closure, Ossification, Pathogenesis, Pigmentation, Reflex, Secondary Growth, Segmentation, Swimming, Translation, Transposition

Quite a number of genes have been found to play important roles in Klippel-feil Syndrome, such as ARHGAP4, C2, C3, C4A, C5, C6, C7, CSF2, CXCL10, GDF6, HNRNPC, LAMC2, PFDN4, PSMA7, RPS26, SS18L1. 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.

Klippel-feil Syndrome Related Genes

click to see detail information for each gene

ARHGAP4 C2 C3
C4A C5 C6
C7 CSF2 CXCL10
GDF6 HNRNPC LAMC2
PFDN4 PSMA7 RPS26
SS18L1