Which are the causes of Sandhoff Disease?

See some of the causes of Sandhoff Disease according to people who have experience in Sandhoff Disease


Sandhoff Disease, also known as GM2 gangliosidosis type 2, is a rare and devastating genetic disorder that primarily affects the nervous system. It is an autosomal recessive disorder, meaning that both parents must carry a mutated gene for the disease to be passed on to their child. Sandhoff Disease is caused by mutations in the HEXB gene, which provides instructions for producing an enzyme called beta-hexosaminidase.



Beta-hexosaminidase is responsible for breaking down a fatty substance called GM2 ganglioside. In individuals with Sandhoff Disease, the HEXB gene mutations lead to a deficiency or complete absence of functional beta-hexosaminidase enzyme. As a result, GM2 ganglioside accumulates in the cells of the brain and spinal cord, leading to progressive damage and dysfunction.



The exact mechanisms by which the accumulation of GM2 ganglioside causes the symptoms of Sandhoff Disease are not fully understood. However, it is believed that the buildup of this substance disrupts normal cellular processes, impairs the function of nerve cells, and ultimately leads to the degeneration of the central nervous system.



There are several known causes of Sandhoff Disease:




  1. Genetic Mutations: Sandhoff Disease is caused by mutations in the HEXB gene. These mutations can occur spontaneously or be inherited from parents who are carriers of the mutated gene. The specific mutations determine the severity and progression of the disease.


  2. Autosomal Recessive Inheritance: Sandhoff Disease follows an autosomal recessive pattern of inheritance. This means that both parents must carry a copy of the mutated HEXB gene to pass it on to their child. If both parents are carriers, there is a 25% chance with each pregnancy that the child will inherit two copies of the mutated gene and develop Sandhoff Disease.


  3. Enzyme Deficiency: The primary cause of Sandhoff Disease is the deficiency or absence of functional beta-hexosaminidase enzyme. This deficiency is a direct result of the genetic mutations in the HEXB gene, which impair the production or function of the enzyme. Without sufficient beta-hexosaminidase, GM2 ganglioside cannot be properly broken down and accumulates in the cells.


  4. GM2 Ganglioside Accumulation: The buildup of GM2 ganglioside in the cells of the brain and spinal cord is a hallmark feature of Sandhoff Disease. The exact mechanisms by which this accumulation leads to the symptoms of the disease are not fully understood, but it is believed to disrupt normal cellular processes and impair the function of nerve cells.


  5. Neurological Degeneration: Over time, the accumulation of GM2 ganglioside and the resulting cellular dysfunction lead to progressive degeneration of the central nervous system. This degeneration affects various regions of the brain and spinal cord, resulting in the wide range of symptoms observed in individuals with Sandhoff Disease.



Sandhoff Disease is a complex genetic disorder with multiple underlying causes. While the specific mechanisms by which the disease develops and progresses are still being studied, the genetic mutations in the HEXB gene and the resulting deficiency of beta-hexosaminidase enzyme play a central role in the pathogenesis of the disease. Understanding these causes is crucial for ongoing research efforts aimed at developing potential treatments and interventions for individuals affected by Sandhoff Disease.


by Diseasemaps

It is created by two parents carrying a mutated gene and passing it on to their offspring cause the disease. Even with both parents carrying the disease in their genome, there is only a 25% chance that they will have a child containing the genetic coding for the disease. Each form of the disease is caused by the differences in the various mutations of the genome, in particular the codons on the 14 exons in the HEX B gene located within chromosome 5 leading to the differences in severities of the symptoms. The difference in the codons has the consequence of inhibiting two enzymes located in the lysosomes of the neurons of the central nervous system. Lysosomes contain various enzymes to break down byproducts and toxins to ensure they do not accumulate enough to interfere with the function of the central nervous system. Using restriction enzymes, it was discovered that a mutation on chromosome 5 particularly within the C1214T allele caused the adult onset form of Sandhoff Disease. For the patient showing symptoms of the infantile or juvenile form they have a mutation on exon I207V from their father, and a 16 base pair deletion from their mother which can be located on as many as 5 exons, exons 1-5.

2/24/17 by Levi Christopher Lucero, Jr. 2185
Translated from spanish Improve translation

For that a thousand people suffer from this disease, mom and dad must be carriers liabilities of the gene of this disease, the two must be carriers, and in each pregnancy there is a 25% chance that the baby appears, the 25% chance on each quest

5/11/17 by Mara. Translated

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