Tay-Sachs disease

Tay-Sachs disease is a rare inherited condition that mainly affects babies and young children. It stops the nerves working properly and is usually fatal.

It used to be most common in people of Ashkenazi Jewish descent (most Jewish people in the UK), but many cases now occur in people from other ethnic backgrounds.

Symptoms

Symptoms of Tay-Sachs disease usually start when a child is 3 to 6 months old.

The main symptoms include:

• being overly startled by noises and movement
• being very slow to reach milestones like learning to crawl, and losing skills they have already learnt
• floppiness and weakness, which keeps getting worse until they're unable to move (paralysis)
• difficulty swallowing
• loss of vision or hearing
• muscle stiffness
• seizures (fits)

The condition is usually fatal by around 3 to 5 years of age, often due to complications of a lung infection (pneumonia).

If you're pregnant or planning a pregnancy, you may be referred to a genetic counsellor to discuss having a test to see if you're at risk of having a child with Tay-Sachs disease and talk about your options.

If your child has possible symptoms of Tay-Sachs disease, a blood test can show if they have it.

Treatments

There's currently no cure for Tay-Sachs disease. The aim of treatment is to make living with it as comfortable as possible.

You'll see a team of specialists, who will help come up with a treatment plan for your child.

Treatments may include:

• medicines for seizures and stiffness
• speech and language therapy for feeding and swallowing problems – sometimes special bottles or a feeding tube may be needed
• physiotherapy to help with stiffness and improve coughing (to reduce the risk of pneumonia)
• antibiotics to treat infections like pneumonia if they occur

Your care team will talk to you about end of life issues, such as where you'd like your child to receive care and if you'd like them to be resuscitated if their lungs stop working.

Further information and advice

You can get more information and support from:

• the Cure & Action for Tay-Sachs (CATS) Foundation
• Climb
• Genetic Alliance UK
• the National Tay-Sachs & Allied Diseases Association (NTSAD) – an American foundation for people with Tay-Sachs disease

If you're interested in finding out more about research into treatments for Tay-Sachs disease, ask your care team about any research you might be able to get involved in.

Information about your child

If your child has Tay-Sachs disease, your clinical team will pass information about him or her on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).

This helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.

Find out more about the register