Tay-Sachs Disease could be a fatal condition
The prevalence of Tay-Sachs disease was traced in Eastern Europe as early as the 18th Century. Doctor Warren Tay, and later, Doctor Bernard Sachs found significant observations about the fatal condition. The cause of the dangerous ailment is hereditary. A child as early as six months old will already show manifestations of the disease. The seriousness of the illness will eventually lead to blindness and death due to the clogging of the nervous system. No known cure has been reported for this dangerous condition.
Tay-Sachs disease is one of the world’s emerging causes of deaths among infants. Indication about the presence of this dreaded medical condition can be identified early during the pregnancy period. A couple of hospital procedures can determine the presence of the disease. During the first 16 to 18 weeks of child expectancy, the method of amniocentesis allows physicians to extract fluid from the abdomen of a pregnant woman. The sample is taken from the vicinity of the unborn child. Medical doctors will examine the fecal cells on the fluid to find a certain vital chemical. The presence of Hex A on the extracted fluid is a big relief, because it concludes that the baby to be born will not be afflicted with the fatal disease. Hex A is a substance that is nowhere to be found on a Tay-Sachs disease. The chorionic villus sampling (CVS) is also a valuable means of identifying the future occurrence of the disease. Physicians insert a tube through the vagina in order to get a fluid sample from the placenta. The chemical is then examined for its presence. This procedure is usually done 10 weeks into pregnancy.
In 1881, a British Ophthalmologist named Warren Tay found red spots in the retina of a patient’s eye. These were the primary symptoms of a degenerative disease which later on was identified as Tay-Sachs disease. As early as the 18th century, the dangerous condition had already manifested among people in Eastern Europe. The disease was known to affect the Jewish population along that area. This was noted by an American neurologist in the person of Bernard Sachs. Cellular changes on the condition were being studied by the specialist closely.
Tay-Sachs Disease Symptoms
As early as six months, symptoms for the disease begin to manifest unknowingly. The stages are set for an infected child to be blinded and paralyzed during the next few months of existence. The fatal condition usually takes its toll before the baby reaches five years old. By then, the toddler who is now blind, inches closer towards an imminent death. Tay-Sachs disease is caused by the absence of a chemical substance that is essential in the breakdown of fatty materials along the nerve areas and in the brain. Without a matter that disposes these fats, deposits will pile up and lead to the clogging of most of the nervous system, which sooner or later shuts itself down. Tay-Sachs disease is hereditary in nature. It is only through the parents that the children can acquire the condition. As of today, no treatment has been recognized for this degenerative health disorder. If you think there is a possibility that you have Tay-Sachs Disease or suffer from the symptoms of Tay-Sachs Disease you should immediately seek medical attention. This particular disease is not something you should mess around with.