Blepharophimosis Syndrome

Overview of Blepharophimosis Syndrome

Most recent studies have shown that Blepharophimosis Syndrome shares some biological mechanisms with blepharophimosis, blepharoptosis, congenital-abnormality, congenital-epicanthus, congenital-ptosis, cytogenetic-abnormality, disorder-of-endocrine-ovary, female-infertility, hypoplasia, infertility, mental-retardation-congenital-heart-disease-blepharophimosis-blepharoptosis-and-hypoplastic-teeth, microcephaly, muscle-hypotonia, neoplasms, ovarian-failure-premature, premature-menopause, tooth-abnormalities, turner-syndrome.

Among the many pathways, these few ones have gauged particular interests from scientists studying Blepharophimosis Syndrome, and have been seen in publications frequently: Aging, Dna Methylation, Hatching, Localization, Menopause, Methylation, Pathogenesis, Regulation Of Gene Expression, Transdifferentiation

Quite a number of genes have been found to play important roles in Blepharophimosis Syndrome, such as ATM, BRD2, CDKN2B, DIAPH2, EGFR, FMR1, FOXL2, HOXA3, HOXA4, MRPL28, NXT1, PLOD1, RP9, SIRT1. 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.

Blepharophimosis Syndrome Related Genes

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Pathways Related to Blepharophimosis Syndrome

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

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