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How are the cause and onset of symptoms of Huntington's disease different from those of PKU and Tay Sachs disease?
Typcially, onset of symptoms with HD is from the mid 30-s to 40's.
What else can I help you with?
How are the cause and onset of symptoms of huntingtons disease different from of PKU and Tay-Sachs disease?
Typcially, onset of symptoms with HD is from the mid 30-s to 40's.
When do symptoms of Tay-Sachs disease first occur?
Symptoms of Tay-Sachs disease develop in infancy and are due to the accumulation of a fatty acid compound in the nervous system.
What are ten genetics diseases?
huntingtons tay sachs cystic fibrosis downs syndrome sickle cell anemia color blindness turner syndrome klinefelter disease alzheimers disease crohns disease
When does tay-sachs disease occur?
Symptoms of Tay-Sachs disease were discovered by Warren Tay in 1881 and Bernard Sachs wrote about it in general in 1887. (this is a disease which affects the brain and eventually kills the person who has it.) Infants that have Tay-Sachs normally die by age 5. They start to lose their functions by the age of 8 months!! Discovered in 1881.
What are some symptoms of Tay-Sachs disease and how can they be identified?
Tay-Sachs disease is a rare genetic disorder that affects the nervous system. Symptoms include developmental delays, loss of motor skills, seizures, and vision and hearing problems. These symptoms can be identified through genetic testing, physical exams, and neurological assessments.
When was Sachs' Disease created?
Sachs' Disease was created in 1999.
Can you get tay sachs disease as an adult?
No, Tay-Sachs disease typically presents in infancy or early childhood. It is a rare genetic disorder that results in the destruction of nerve cells in the brain and spinal cord. Adults who carry the gene mutation for Tay-Sachs disease do not develop symptoms of the disease themselves, but may pass the gene on to their children.
What are the symptoms of Tay-Sachs disease and how do they manifest in affected individuals?
Tay-Sachs disease is a rare genetic disorder that affects the nervous system. Symptoms typically appear in infancy and include developmental delays, muscle weakness, loss of motor skills, and seizures. As the disease progresses, affected individuals may experience vision and hearing loss, intellectual disability, and paralysis. Unfortunately, there is currently no cure for Tay-Sachs disease, and it often leads to premature death in childhood.
Tay-Sachs disease is a human?
Tay-Sachs disease is a human genetic disorder.
What effect does Tay Sachs disease have on the body?
what effect does Tay-sachs disease have on the body?
What system or part of the body does tay sachs disease affect?
what effect does Tay-sachs disease have on the body?
A person can be tested for the allele that causes Tay-Sachs disease because the what of that allele is different from that of the normal allele?
The DNA sequence of the allele that causes Tay-Sachs disease is different from that of the normal allele. This difference in the DNA sequence allows for specific genetic tests to be conducted to identify the presence of the Tay-Sachs disease allele in individuals.
