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Disease Info Card
Menkes Kinky Hair Syndrome
Information about Menkes Kinky Hair 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 Menkes Kinky Hair Syndrome
Most recent studies have shown that Menkes Kinky Hair Syndrome shares some biological mechanisms with atrophy, brain-diseases, brain-diseases-metabolic, copper-deficiency, copper-metabolism-disorder, cutis-laxa, cutis-laxa-x-linked, ehlers-danlos-syndrome, epilepsy, growth-disorders, hair-diseases, hepatolenticular-degeneration, hereditary-diseases, inborn-errors-of-metabolism, nerve-degeneration, nervous-system-disorder, nervousness, neurodegenerative-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Menkes Kinky Hair Syndrome, and have been seen in publications frequently: Angiogenesis, Brain Development, Cell Death, Endocytosis, Excretion, Glycosylation, Golgi Localization, Intestinal Absorption, Lactation, Localization, Methylation, Myelination, Pathogenesis, Pigmentation, Pinocytosis, Reverse Transcription, Secretion, Secretory Pathway, Translation, Transport
Quite a number of genes have been found to play important roles in Menkes Kinky Hair Syndrome, such as ATOX1, ATP7A, ATP7B, CALCR, CP, CYCS, DBH, ELN, LOX, MCAT, PAM, SLC31A1, TG, TYR. 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.