Juvenile Tay-Sachs Disease

mutation in alpha subunit of hexosaminidase A

Also Known As:

Tay-Sachs Disease, Juvenile

Networked: 3 relevant articles (0 outcomes, 0 trials/studies)

1.	Tremor (Tremors)
2.	Tay-Sachs Disease
3.	Sandhoff Disease (Sandhoff's Disease)

Drugs and Important Biological Agents (IBA) related to Juvenile Tay-Sachs Disease:

1.	Hexosaminidase A (Hex A)IBA 05/01/2022 - "Juvenile Tay Sachs Disease Due to Compound Heterozygous Mutation in Hex-A Gene, with Early Sign of Bilateral Tremors." 04/01/1986 - "Two have juvenile Tay-Sachs disease with hexosaminidase A deficiency and three have juvenile Sandhoff disease with hexosaminidase A and B deficiency. "
2.	Messenger RNA (mRNA)IBA 06/01/2010 - "We have identified three mutations in the beta-hexoseaminidase A (HEXA) gene in a juvenile Tay-Sachs disease (TSD) patient, which exhibited a reduced level of HEXA mRNA. "