Bloom Syndrome, otherwise known as Bloom-Torre-Machacek syndrome or congenital telangiectatic erythema, is a hereditary disorder identified by short stature, sun-sensitive skin changes, an increased risk of cancer, and other related health problems. Bloom Syndrome is most commonly seen in people of Central and Eastern European Jewish background, which occurs in about 1 in 50,000 people however Bloom Syndrome can affect men or women and is diagnosed using blood samples. This disorder is not life-threatening itself however the elevated rate of mutation in Bloom Syndrome results in a high risk of cancer in affected individuals.
Bloom Syndrome Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Bloom Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 747 products for the study of Bloom Syndrome that can be applied to Chromatin Immunoprecipitation, Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Chromatin Immunoprecipitation (ChIP), Immunohistochemistry from our catalog of antibodies and ELISA kits.
Bloom Syndrome is also known as bloom syndrome, congenital telangiectatic erythema, growth deficiency, sun-sensitive, telangiectatic, hypo and hyperpigmented skin, predisposition to malignancy and chromosomal instability, congenital telangiectatic erythema syndrome, neonatal hemochromatosis, bls, blm, bs.