Disease Info Card

Hydranencephaly

Information about Hydranencephaly: 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 Hydranencephaly

Most recent studies have shown that Hydranencephaly shares some biological mechanisms with acquired-porencephaly, anencephaly, arthrogryposis, bluetongue, brain-diseases, cattle-diseases, congenital-abnormality, congenital-absence, congenital-cerebellar-hypoplasia, dysplasia, fetal-death, fetal-diseases, holoprosencephaly, hydrocephalus, hypoplasia, microcephaly, nervousness, pregnancy-complications-infectious, sheep-diseases, virus-diseases.

Among the many pathways, these few ones have gauged particular interests from scientists studying Hydranencephaly, and have been seen in publications frequently: Associative Learning, Brain Development, Cell Cycle, Cell Cycle Arrest, Cell Division, Cell Migration, Chromosome Breakage, Coagulation, Habituation, Heart Formation, Inflammatory Response, Mating, Neural Crest Cell Development, Pathogenesis, Reflex, Reverse Transcription, Secretion, System Development, Transposition, Tropism

Quite a number of genes have been found to play important roles in Hydranencephaly, such as ACP5, ARX, CD40LG, CRAT, CSF2, ENO2, ERG, FGFR3, FLVCR2, LAMC2, PRL, SCYL1, TDRD7, TNFSF14, UBA2. 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.