Tay-Sachs disease digital illustration

Tay-Sachs disease Save


ICD-10 code: E75.02

Disease category: E75.0: GM2 gangliosidosis

Tay-Sachs Disease: Understanding the Rare Genetic Disorder

Tay-Sachs disease is a rare genetic disorder that affects the nerve cells in the brain and spinal cord. It is caused by a genetic mutation that results in the deficiency of an enzyme called hexosaminidase A (Hex-A). This deficiency leads to the accumulation of a fatty substance called GM2 ganglioside in the nerve cells, causing progressive damage.

Here are some key facts about Tay-Sachs disease:

  1. Tay-Sachs is an autosomal recessive disorder, meaning both parents must carry the defective gene for a child to be affected.
  2. It primarily affects infants and young children, with symptoms usually appearing around 3 to 6 months of age.
  3. Early signs of Tay-Sachs disease include developmental delays, muscle weakness, and an exaggerated startle response.
  4. As the disease progresses, children may experience seizures, vision and hearing loss, and difficulties with movement.
  5. Unfortunately, Tay-Sachs disease is progressive and currently has no cure.

Diagnosis of Tay-Sachs disease typically involves a blood test to measure the levels of Hex-A enzyme activity. Additionally, genetic testing can identify carriers of the Tay-Sachs gene.

It is important to note that Tay-Sachs disease is more prevalent among certain ethnic groups, including Ashkenazi Jews, French-Canadians, and Cajuns of Louisiana. However, it can affect individuals from any ethnic background.

Although there is no cure for Tay-Sachs disease, supportive care can help manage the symptoms and improve the quality of life for affected individuals. This may involve physical and occupational therapy, medications to control seizures, and interventions to address feeding difficulties.

In conclusion, Tay-Sachs disease is a rare genetic disorder characterized by the accumulation of GM2 ganglioside in nerve cells. It primarily affects infants and young children and currently has no cure. Early diagnosis and supportive care are crucial in managing the symptoms and improving the quality of life for those affected by this devastating condition.

Treatment of Tay-Sachs disease:

Treatment Options for Tay-Sachs Disease

Tay-Sachs disease is a rare genetic disorder that affects the nervous system. It is caused by the absence or malfunctioning of a specific enzyme called hexosaminidase A (Hex A). Currently, there is no known cure for this devastating condition. However, there are treatment options available that can help manage the symptoms and improve the qua...

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