Disease Info Card

Arnold Chiari Malformation

Information about Arnold Chiari Malformation: 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 Arnold Chiari Malformation

Most recent studies have shown that Arnold Chiari Malformation shares some biological mechanisms with apnea, brain-diseases, chiari-malformation-type-i, congenital-abnormality, congenital-cerebral-hernia, headache, hernia, hernia-of-cerebellar-tonsil-into-foramen-magnum, hydrocephalus, intracranial-hypertension, meningomyelocele, neoplasms, nervousness, nystagmus, pain, platybasia, scoliosis-unspecified, spina-bifida, spinal-cord-diseases, syringomyelia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Arnold Chiari Malformation, and have been seen in publications frequently: Brain Development, Cell Death, Cell Proliferation, Central Nervous System Development, Coagulation, Dehiscence, Innervation, Localization, Muscle Atrophy, Myelination, Neural Tube Closure, Ossification, Pathogenesis, Proprioception, Reflex, Regeneration, Segmentation, Transport, Transposition, Tube Closure

Quite a number of genes have been found to play important roles in Arnold Chiari Malformation, such as ARHGAP4, AVP, C2, C3, C5, CFD, CFP, CSF2, CXCL10, FLNA, GFAP, HNRNPC, LAMC2, NLRP5, PFDN4, PPOX. 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.