Turner Syndrome is a condition that only affects women, and occurs when one X chromosome is partially or completely missing. Turner Syndrome is the result of a random chromosomal abnormality that occurs before or during fertilization. Most individuals with Turner Syndrome are short in height. If the individual is diagnosed before they stop growing, hormone therapy can be utilized to allow the girl to grow taller and undergo puberty. Other symptoms include a low hairline at the back of the neck, abnormal bone development, drooping eyelids, kidney problems, high blood pressure, diabetes, and thyroid problems. Most individuals are infertile due to ovarian tissue degeneration before birth. Turner syndrome is diagnosed by examining a karyotype. Turner Syndrome cannot be cured, but specific symptoms can be treated, especially if the condition is recognized during early childhood.
Turner 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 Turner Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 1472 products for the study of Turner Syndrome that can be applied to Western Blot, Chromatin Immunoprecipitation, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Turner Syndrome is also known as turner syndrome, bonnevie-ullrich syndrome, ullrich-turner syndrome, 45,x, ts, bonnevie-ullrich syndrome nos (disorder), turner's syndrome nos (disorder), gonadal dysgenesis turner type, bonnevie-ullrich syndrome nos, schereshevkii turner syndrome, gonadal dysgenesis - turner, turner syndrome (disorder), gonadal dysgenesis (45,x), bonnevie-ulrich syndrome, chromosome x monosomy x, turner varny syndrome, turner's syndrome nos, monosomy x syndrome, gonadal dysgenesis, turner's syndrome, karyotype 45, x, 45, x syndrome, xo syndrome.
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