Diagnosis typically involves clinical evaluation, genetic testing to identify mutations in the HEXB gene, and biochemical tests to measure hexosaminidase activity in the blood or tissue.
How is Sandhoff disease diagnosed?
Share This Story, Choose Your Platform!
About the Author: Staff Writer
World Eyecare Foundation staff writers are experienced eye care providers, researchers, academicians, industry leaders and practicing ophthalmologists and optometrist from around the world. Content may be generated by AI and is reviewed by the editorial team and specialists in the areas of publications.
Leave A Comment