Search Results 1-10 of 26129 for Tay-Sachs disease
The genetic change that causes Tay-Sachs disease results in a deficiency of the enzyme beta-hexosaminidase A. This enzyme is required to break down the fatty ...
To confirm that your child has Tay-Sachs disease, your health care provider will ask about symptoms and any family hereditary disorders, and also do a physical ...
In hindsight, these events were early signs that twins Katie and Allie Buryk had late onset Tay-Sachs disease, a rare genetic disorder. But it wasn't until ...
... Tay-Sachs disease and other rare neurological diseases. Nationally recognized expertise. Every year, Mayo Clinic's experts diagnose and care for children who ...
See a list of publications about Tay-Sachs disease by Mayo Clinic doctors on PubMed, a service of the National Library of Medicine. Research Profiles. Edit ...
The purpose of this study is to assess the safety and effectiveness of N-Acetyl-L-Leucine (IB1001) for the treatment of GM2 Gangliosidosis (Tay-Sachs and ...
A Study to Evaluate the Effects of N-Acetyl-L-Leucine for GM2 Gangliosdisosis (Tay-Sachs and Sandhoff Disease) ... (Tay-Sachs and Sandhoff Disease). Participation ...
Tay-Sachs disease · Tension headache; Thalamic pain; Third nerve palsy; Thoracic outlet syndrome; Thoracic radiculopathy; Thunderclap headaches; Tics; Tingling ...
Tay-Sachs disease. Wilson's disease. When to see a doctor. If you have concerns about your child's growth and development or your own health, talk to your ...
An enzyme that breaks down certain fatty substances doesn't work properly in people with Gaucher disease. Enzyme replacement therapy often helps.
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