Interparietal Craniosynostosis

Overview of Interparietal Craniosynostosis

Most recent studies have shown that Interparietal Craniosynostosis shares some biological mechanisms with acrocephaly, blood-loss-surgical, congenital-abnormal-synostosis, congenital-abnormality, congenital-heart-defects, craniofacial-dysostosis, craniosynostosis, developmental-disabilities, dysplasia, frontal-bossing, hematoma, hemorrhage, hydrocephalus, intracranial-hypertension, learning-disorders, low-set-ears, plagiocephaly, scaphycephaly, skull-malformation.

Among the many pathways, these few ones have gauged particular interests from scientists studying Interparietal Craniosynostosis, and have been seen in publications frequently: Brain Development, Endochondral Ossification, Intramembranous Ossification, Localization, Ossification, Pathogenesis, Wound Healing

Quite a number of genes have been found to play important roles in Interparietal Craniosynostosis, such as ACE, ACSS2, CSF2, FGFR1, FGFR2, FGFR3, NANS, NDUFB6, NLRP5, NOG, NTM, PADI1, PLA2G15, RNF7, SNRPE, TCF21, TSPAN31, TWIST1, VDAC2. 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.

Interparietal Craniosynostosis Related Genes

click to see detail information for each gene

Pathways Related to Interparietal Craniosynostosis

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

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