Symptoms
A baby with
Tay-Sachs disease has no signs or symptoms of the
disease at birth. Symptoms usually appear 3 to 6 months after birth. The
symptoms are caused by damage to the brain and nerve cells from the buildup of
fatty compounds. An early sign of the infantile form of Tay-Sachs is a red spot
on the
retina. See an illustration of the
retina
.
Watch for the following symptoms if you suspect your baby may have
Tay-Sachs disease.
At 3 to 6 months, you may notice:
- Decreased eye contact.
- Twitchy
eyes (myoclonic jerks).
- Difficulty focusing on
objects.
- Excessively startled by sharp but not necessarily loud
noises.
At 6 to 10 months, you may notice:
- Limp and floppy muscles
(hypotonia).
- Decreased alertness and
playfulness.
- Difficulty sitting up or rolling over and a loss of
motor skills.
- Decreased hearing and eventual deafness.
-
Gradual loss of vision.
- An abnormal increase in head size
(macrocephaly).
10 months and older
As a child with Tay-Sachs grows older, he or she may become
blind, mentally retarded, paralyzed, and unresponsive to the environment. The
child also may have
seizures, difficulty swallowing, and difficulty
breathing. Children with Tay-Sachs disease rarely live beyond 4 or 5 years of
age.
Late-onset Tay-Sachs disease
Symptoms of
late-onset Tay-Sachs disease (LOTS) usually develop
between adolescence and the mid-30s. The symptoms vary among individuals,
depending on the amount of hex A being produced by the body. At first, symptoms
such as clumsiness or mood changes are subtle and may go unnoticed. Other
symptoms that may develop include:
- Personality changes.
- Muscle
weakness or twitching.
- Slurred speech.
- Impaired
thinking and reasoning ability, such as memory problems, difficulty with
comprehension, and short attention span.
- Inability to distinguish
between what's real and unreal (psychotic episodes) or
depression.